Patent Application
20100069303
1. Field of the Invention
The present invention relates generally to the fields of cancer research and targeted therapy. More specifically, the present invention relates to fusion constructs comprising an isoform of vascular endothelial growth factor and uses of such constructs.
2. Description of the Related Art
Vascular endothelial growth factor (VEGF)-A plays a central role in the growth and metastasis of solid tumors, and acts as a primary stimulant of vascularization in solid tumors. VEGF-A enhances endothelial cell proliferation, migration, and survival and is essential for blood vessel formation. Other roles of vascular endothelial growth factor include wound healing, vascular permeability and the regulation of blood flow. Through alternative splicing of RNA, human vascular endothelial growth factor exists as at least four isoforms of 121, 165, 189, or 206 amino acids. The lowest molecular weight isoform, designated VEGF121, is a non-heparan sulfate-binding isoform that exists in solution as a disulfide-linked homodimer.
VEGF is released by a variety of tumor cells. The angiogenic actions of VEGF are mediated through two related receptor tyrosine kinases, kinase domain receptor (KDR) and FLT-1 in the human, and Flk-1 and Flt-1 in the mouse. Both are largely restricted to vascular endothelial cells. KDR/Flk-1 and FLT-1 receptors are overexpressed on the endothelium of tumor vasculature. In contrast, these receptors are almost undetectable in the vascular endothelium of adjacent normal tissues. The receptors for vascular endothelial growth factor thus seem to be excellent targets for the development of therapeutic agents that inhibit tumor growth and metastatic spread through inhibition of tumor neovascularization.
To this end, VEGF121 would be an appropriate carrier to deliver a toxic agent selectively to tumor vascular endothelium. VEGF121 exists in solution as a disulfide linked homodimer and binds to KDR and FLT-1 in a heparin-independent manner. It does not bind neuropilin-1 or neuropilin-2. VEGF121 has been shown to contain the full biological activity of the larger variants.
Molecular engineering enabled the synthesis of novel chimeric molecules having therapeutic potential. Chimeric fusion constructs targeting the IL-2 receptor, the EGF receptor, and other growth factor/cytokine receptors have been described. It has also been showed that a chemical conjugate of vascular endothelial growth factor and truncated diphtheria toxin has impressive cytotoxic activity on cell lines expressing receptors for vascular endothelial growth factor. Further studies with VEGF/diphtheria toxin fusion constructs demonstrated selective toxicity to Caprice's sarcoma cells and dividing endothelial cells in vitro and in vivo. However, the prior art is deficient in fusion constructs comprising vascular endothelial growth factor and other cytotoxic molecule with improved biochemical and pharmacological properties. The present invention fulfills this long-standing need and desire in the art.
The present invention discloses targeting of neovasculature of solid tumors with a chimeric fusion toxin comprising the 121-amino acid isoform of vascular endothelial growth factor (VEGF121). In one embodiment, the chimeric fusion toxin (VEGF121/rGel) consists of VEGF121 and recombinant gelonin (rGel), a low molecular weight single chain toxin with a mechanism of action similar to that of ricin A-chain. VEGF121 is linked by a flexible G4S tether to the toxin gelonin and expressed as a soluble protein in bacteria. Both VEGF121/rGel and VEGF121 stimulated cellular kinase domain receptor (KDR) phosphorylation. The VEGF121/rGel fusion construct was highly cytotoxic to endothelial cells overexpressing the KDR/Flk-1 receptor. Endothelial cells overexpressing FLT-1 were not sensitive to the fusion protein.
While several studies have shown both receptors of VEGF121, namely VEGFR-1 (FLT-1) and VEGFR-2 (KDR/Flk-1), to be over-expressed on the endothelium of tumor vasculature, the present invention reports several surprising results which demonstrate that VEGF121/rGel has several advantageous properties. Cell ELISA using antibodies specific to either KDR or FLT-1 indicate binding of VEGF121/rGel to both receptors. While VEGF121/rGel binds to both FLT-1 and KDR, internalization of VEGF121/rGel is mediated only by KDR and not FLT-1.
Experiments with human melanoma, human prostate tumor or bladder tumor xenografts demonstrate successful use of VEGF121/rGel fusion construct for the targeted destruction of tumor vasculature in viva The present invention also indicates that the anti-tumor vascular-ablative effect of VEGF121/rGel may be utilized not only for treating primary tumors but also for inhibiting metastatic spread and vascularization of metastases. Taken together, these results indicate that selective destruction of tumor vasculature can be achieved with VEGF121/rGel in mice, giving impressive antitumor effects. Gross morphological toxicity to normal organs was not visible in animals treated with a therapeutic dose. Therefore, VEGF121/rGel is a potential antitumor agent useful for treating cancer patients.
In another embodiment, there is provided a chimeric fusion toxin (GrB/VEGF121) consisting of VEGF121 and granzyme B (GrB), a serine protease capable of inducing apoptosis through both caspase-dependent and caspase-independent pathways. GrB/VEGF121 induced apoptotic events specifically on FLK-1-expressing porcine aortic endothelial cells as assessed by terminal deoxynucleotidyl transferase-mediated nick end labeling assay, DNA laddering, and cytochrome c release from mitochondria. In addition, the fusion construct mediated cleavage of caspase-8, caspase-3, and poly(ADP-ribose) polymerase in target endothelial cells within 4 h after treatment. In conclusion, delivery of the human proapoptotic pathway enzyme granzyme B to tumor vascular endothelial cells or to tumor cells may have significant therapeutic potential and represents a potent new class of targeted therapeutic agents with a unique mechanism of action.
Thus, the present invention is directed to compositions of matter comprising a conjugate comprising an isoform of vascular endothelial growth factor (VEGF) and a cytotoxic molecule. In another embodiment, the conjugate comprises a cytotoxic molecule and a peptide that binds to both VEGF receptor type 1 (Flt-1) and VEGF receptor type 2 (kinase domain receptor/Flk-1). In general, the cytotoxic molecule is a toxin such as gelonin or a molecule that induces apoptosis such as granzyme B.
In another embodiment of the present invention, there are provided methods of killing cells expressing type 2 or type 1 VEGF receptors by the present conjugates which are internalized by VEGF receptor type 2 or type 1 respectively.
In yet another embodiment, there are provided methods of using the conjugates of the present invention to inhibit tumor growth, metastatic spread or vascularization of metastases in an animal or a human.
The present invention further provides methods of using the conjugates of the present invention to inhibit osteoclastogenesis or angiogenesis in an animal or a human.
Other aspects, features, and advantages of the present invention will be apparent from the following description of the presently preferred embodiments of the invention. These embodiments are given for the purpose of disclosure.
The expression of vascular endothelial growth factor and its receptors has been closely linked to tumor vascularity, metastasis, and progression. Several groups have developed anti-angiogenic drugs that block kinase activity of the vascular endothelial growth factor receptors or monoclonal antibodies that block vascular endothelial growth factor-receptor interactions. The present invention demonstrates chimeric fusion constructs containing the 121-amino acid isoform of vascular endothelial growth factor (VEGF121) and a cytotoxic molecule such as plant toxin gelonin or serine protease granzyme B.
Agents targeting the neovascularization process in tumors have significant potential for therapeutic impact. Molecules which interfere with the growth and development of vascular endothelial cells by targeting the VEGF/receptor complex have an additional advantage since these agents do not have to penetrate into the tumor parenchyma and the receptor targets are expressed on the luminal surface of tumor vascular endothelium.
Possible binding of vascular endothelial growth factor-containing constructs to the neuropilin receptor could be a source of unwanted toxicity and mis-targeting of the complex; however, it has been shown that the VEGF121 fragment as opposed to other isoforms of VEGF-A does not appear to bind to this receptor.
It is specifically contemplated that pharmaceutical compositions may be prepared using the novel fusion constructs of the present invention. In such a case, the pharmaceutical composition comprises the novel fusion constructs of the present invention and a pharmaceutically acceptable carrier. A person having ordinary skill in this art would readily be able to determine, without undue experimentation, the appropriate dosages and routes of administration of this fusion toxin of the present invention. When used in vivo for therapy, the fusion construct of the present invention is administered to the patient or an animal in therapeutically effective amounts, i.e., amounts that eliminate or reduce the tumor burden or other desired biological effects. It will normally be administered parenterally, preferably intravenously, but other routes of administration will be used as appropriate.
The dose and dosage regimen will depend upon the nature of the disease or cancer (primary or metastatic) and its population, the characteristics of the particular fusion toxin, e.g., its therapeutic index, the patient, the patient's history and other factors. The amount of fusion toxin administered will typically be in the range of about 0.01 to about 100 mg/kg of patient weight. The schedule will be continued to optimize effectiveness while balanced against negative effects of treatment. See Remington's Pharmaceutical Science, 17th
Ed. (1990) Mark Publishing Co., Easton, Pa.; and Goodman and Gilman's: The Pharmacological Basis of Therapeutics, 8th Ed. (1990) Pergamon Press. For parenteral administration, the fusion toxin protein will most typically be formulated in a unit dosage injectable form (solution, suspension, emulsion) in association with a pharmaceutically acceptable parenteral vehicle. Such vehicles are preferably non-toxic and non-therapeutic. Examples of such vehicles are water, saline, Ringer's solution, dextrose solution, and 5% human serum albumin. Non-aqueous vehicles such as fixed oils and ethyl oleate may also be used.
Liposomes may be used as carriers. The vehicle may contain minor amounts of additives such as substances that enhance isotonicity and chemical stability, e.g., buffers and preservatives. The fusion toxin will typically be formulated in such vehicles at concentrations of about 0.01 mg/ml to 1000 mg/ml.
The present invention is directed to a composition of matter comprising a conjugate comprising a cytotoxic molecule and a peptide that binds to both VEGF receptor type 1 (Flt-1) and VEGF receptor type 2 (kinase domain receptor/Flk-1). In one embodiment, the peptide is an isoform of VEGF such as those having a sequence of SEQ ID NOs:28-34. In general, the cytotoxic molecule is a toxin such as gelonin or a signal transduction protein capable of generating apoptotic signals. Representative signal transduction proteins for apoptosis induction include granzyme B, Bax, TNF-a, TNF-b, TNF-like molecule, TGF-b, small interfering RNA, IL-12, IL-3, IL-24, IL-18, TRAIL, IFN-a, IFN-b, IFN-g, Bcl-2, Fas ligand and caspases. In one embodiment, the conjugate is a fusion protein of the 121-amino acid isoform of VEGF (VEGF121) and a cytotoxic molecule. For example, the fusion protein may include a linker such as G4S, (G4S)2, the 218 linker, (G4S)3, enzymatically cleavable linker, pH cleavable linker or any similar linker well known to a person having ordinary skill in this art.
In addition to the 121-amino acid isoform of VEGF, the present invention encompasses other peptides that bind to both VEGF receptor type 1 and type 2. A number of such peptides have been reported. For example, peptides binding type 2 VEGF receptor can be identified by screening with membrane-expressed type 2 VEGF receptors or with anti-VEGF neutralizing monoclonal antibody (Binetruy-Tournaire et al., 2000; Wu et al., 2002). A heterodimeric VEGF antagonist comprising binding domains for VEGF receptor type 1 and type 2 at one pole of the dimer has been shown to block VEGF receptor type 1- and type 2-mediated activities (Leenders et al., 2002). Moreover, VEGF receptor-targeting peptides can be high affinity antibodies selected from phage display library (Lu et al., 2003).
In another embodiment, there is provided a method of using the conjugates of the present invention to kill cells expressing type 2 VEGF receptors (kinase domain receptor/Flk-1 receptors). The conjugate can bind to both VEGF receptor type 1 (Flt-1) and VEGF receptor type 2 (KDR/Flk-1) but is internalized by VEGF receptor type 2 expressed on the cells. In general, the conjugate is cytotoxic to cells expressing more than 2000 type 2 VEGF receptors per cell. Examples of cells that are susceptible to the claimed conjugate include prostate tumor cells, breast cancer cells and bladder tumor cells.
In another embodiment, there is provided a method of using the conjugates of the present invention to kill cells expressing type 1 VEGF receptors. The conjugate can bind to both VEGF receptor type 1 (Flt-1) and VEGF receptor type 2 (KDR/Flk-1) but is internalized by VEGF receptor type 1 expressed on the cells. Examples of cells that are susceptible to the claimed conjugate include osteoclast precursor cells.
In yet another embodiment, there is provided a method of using the claimed conjugates to inhibit tumor growth, metastatic spread or vascularization of metastases in a subject. As used herein, a “subject” refers to an animal or a human. The method involves using a biologically effective amount of the claimed conjugates to exert cytotoxic effect on the tumor vasculature. The method may further comprise treatment with chemotherapeutic agents or radiotherapeutic agents well known in the art.
The present invention further provides methods of using the claimed conjugates to inhibit osteoclastogenesis, angiogenesis or to treat bone disease such as osteoporosis and osteoarthritis in an animal or a human.
In yet another embodiment, there is provided a method of inducing a cytotoxic effect or an anti-tumor effect such as inhibition of tumor growth, metastatic spread or vascularization of metastases. The method comprises the step of inducing expression of one or more genes listed in Table 4.
The following examples are given for the purpose of illustrating various embodiments of the invention and are not meant to limit the present invention. The present examples, along with the methods, procedures, treatments, and specific compounds described herein are representative of preferred embodiments. One skilled in the art will appreciate that the present invention is well adapted to carry out the objects and obtain the advantages mentioned, as well as those objects, ends and advantages inherent herein. Changes therein and other uses which are encompassed within the spirit of the invention as defined by the scope of the claims will occur to those skilled in the art.
Endothelial cell growth supplement from bovine neural tissue was obtained from Sigma. Murine brain endothelioma bEnd.3 cells were provided by Werner Risau (Max Plank Institute, Munich, Germany). Porcine aortic endothelial cells (PAE) transfected with either the human FLT-1 receptor (PAE/FLT-1) or the KDR receptor (PAE/KDR) were provided by Dr. J. Waltenberger. Soluble mouse Flk-1 was expressed in Sf9 cells as described by Warren et al. (1995). The human melanoma A-375 M cell line, human breast cancer SKBR3-HP, and HuT-78 cells were obtained from American Type Culture Collection. Tissue culture reagents were from GIBCO/BRL or Mediatech Cellgro (Herndon, Va.).
Rabbit anti-gelonin antisera was obtained from the Veterinary Medicine Core Facility at M.D. Anderson Cancer Center. Anti-flt-1 (sc-316), anti-flk-1 (sc-504), and anti-PARP (sc-8007) antibodies were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, Calif.). BALB/c nude mice were purchased from The Jackson Laboratory and maintained under sterile pathogen-free conditions according to American Association of Laboratory Animal Care standards.
Anti-granzyme B mouse monoclonal antibody, and anti-caspase antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, Calif.). Horseradish peroxidase-goat anti-mouse (HRP-GAM) or anti-rabbit conjugate were purchased from Bio-Rad (Hercules, Calif.). FITC-coupled anti-mouse IgG was obtained from Sigma Chemical Co. (St. Louis, Mo.). Cytochrome c release apoptosis assay kit was purchased from Oncogene Research Products (Boston, Mass.). In situ cell death detection kit, AP [terminal deoxynucleotidyl transferase-mediated nick end labeling (TUNEL) assay], and Fast Red were from Roche Molecular Biochemicals (Indianapolis, Ind.).
The PCR reagents were obtained from Fisher Scientific, and the molecular biology enzymes were purchased from Roche Molecular Biochemicals or New England Biolabs. Bacterial strains, pET bacterial expression plasmids, and recombinant enterokinase were obtained from Novagen. All other chemicals were obtained from Sigma or Fisher Scientific. Metal affinity resin (Talon) was obtained from CLONTECH. Other chromatography resin and materials were purchased from Amersham Pharmacia.
Construction of VEGF121/rGelonin Fusion Toxin
The cDNA encoding human VEGF121 and recombinant gelonin were fused together by using the splice overlap extension PCR method with VEGF and gelonin DNA as templates. Primers used were: VEGF Nterm, (5′-TGGTCCCAGGCTCATATGGCA CCCATGGCAGAA-3′, SEQ ID NO:1); VEGF Cterm, (5′-TCTAGACCGGAGCCACCGCCACCCCGCCTCGGCTTGTC-3′, SEQ ID NO:2); Gel Nterm, (5′-GGTGGCGGTGG CTCCGGTCTAGACACCGTGAGC-3′, SEQ ID NO:3); Gel Cterm, (5′-AAGGCTCGTGTCGACCTCGAGTCATTAAGCTTTAGGAT CTTTATC-3′, SEQ ID NO:4). A G4S linker was incorporated between the VEGF121 and the rGel sequences. Purified PCR products were digested with the restriction enzymes BspHI and XhoI and ligated into pET-32a. The constructs were transformed into Escherichia coli strain AD494 (DE3) pLys S for expression of the fusion protein.
The combination of VEGF121 and recombinant gelonin was originally prepared in two different orientations (
VEGF121/rGelonin Expression in E. Coli and Purification
The expression and purification of VEGF121/rGel has been previously described (Veenendaal et al., 2002). Bacterial colonies transformed with the plasmid carrying the VEGF121/rGel insert were cultured in LB growth medium (Sigma) containing 200 mg/ml ampicillin, 70 mg/ml chloramphenicol, and 15 mg/ml kanamycin at 37° C. overnight in a shaker bath at 240 rpm. The cultures then were diluted 1:20 with fresh LB medium with antibiotics and grown to early log phase (A600/0.6) at 37° C. Thereafter, the cultures were diluted 1:1 with fresh LB medium plus antibiotics. Protein synthesis was induced at 23° C. by the addition of 0.1 mM isopropyl b-D-thiogalactoside (IPTG) overnight. The cells were collected by centrifugation, resuspended in 10 mM Tris/HCl (pH 8.0), and frozen.
The fusion protein was expressed and purified from bacterial supernatant. E. coli cells were lysed with 100 ml 0.1 mm glass beads (BioSpec Products, Inc) in a Bead Beater (BioSped Products, Inc) for eight cycles of 3 minutes each. The lysate was ultracentrifuged at 40,000 rpm for 90 minutes at 4° C. The supernatant was carefully collected and adjusted to 40 mM Tris-HCl (pH 8.0), 300 mM NaCl, and incubated at 4° C. with metal affinity resin. The resin was washed with 40 mM Tris-HCl (pH8.0), 0.5 M NaCl buffer containing 5 mM Imidazole and eluted with buffer containing 100 mM Imidazole. After pooling fractions containing VEGF121/rGel, the sample was dialyzed against 20 mM Tris (pH 8.0), 200 mM NaCl and digested with recombinant Enterokinase at room temperature. Enterokinase was removed by agarose-linked soybean trypsin inhibitor. Other proteins of non-interest were removed by Q Sepharose Fast Flow resin and metal affinity resin as described previously26. VEGF121/rGel was concentrated and stored in sterile PBS at −20° C.
SDS/PAGE analysis of protein expression after induction with IPTG showed a new protein at 62 kDa, which is the expected molecular weight for the fusion protein plus the 21 kDa purification tag. This material was purified by binding and elution from IMAC resin. Cleavage with recombinant enterokinase removed the tag resulting in a 42-kDa protein under reducing conditions. The construct migrated as a homodimer at 84 kDa under nonreducing conditions. The fusion construct was immunoreactive with antibodies to both VEGF and rGel. One liter of induced bacterial culture initially contained ˜2,000 mg of soluble fusion construct. Initial IMAC purification resulted in 750 mg of VEGF121/rGel product (yield 37.5%), and digestion with recombinant enterokinase generated 400 mg of target protein (yield 20%). Subsequent purification yielded 230 mg of VEGF121/rGel final product (11.5% overall yield).
Protein samples were analyzed by SDS/15% PAGE under reducing conditions. The gel was electrophoretically transferred to nitrocellulose overnight at 4° C. in transfer buffer (25 mM Tris/HCl, pH 7.6/190 mM glycine/20% HPLC-grade methanol). The membranes were blocked by the addition of 5% BSA in Western blocking buffer [(TBS)/Tween] and then incubated for 1 h with rabbit anti-gelonin polyclonal antibody (2 mg/ml in TBS/Tween) or mouse anti-VEGF monoclonal antibody 2C3 (2 mg/ml in TBS/Tween). The membrane then was incubated with goat-anti-rabbit IgG horseradish peroxidase (HRP) or goat-anti-mouse IgG-HRP (1:5,000 dilution in TBS/Tween). Then, the membrane was developed with the Amersham Pharmacia enhanced chemiluminescence (ECL) detection system and exposed to x-ray film.
Biological Activity of the rGel Component
The functional activity of rGel and VEGF121/rGel were assayed by using a cell-free protein translation inhibition assay kit from Amersham Pharmacia as described by the manufacturer. As determined by the rabbit reticulocyte translation assay, the purified VEGF121/rGel and rGel had IC50 values of ˜47 and 234 pM, respectively, showing that fusion of rGel and VEGF121 did not reduce the activity of the toxin component (
Binding of VEGF121/rGelonin to Soluble Flk-1 Receptor
Binding to Flk-1 was tested on microtiter plates coated with soluble mouse Flk-1. Plates were treated with 2 mg/ml of NeutrAvidin (Pierce) for 6 h. Purified, biotinylated Flk-1 (Warren et al., 1995) was incubated with NeutrAvidin-coated wells for 2 h. VEGF121 or VEGF121/rGel was added to the wells at various concentrations in the presence of PBS containing 2% (vol/vol) BSA. After 2 h of incubation, plates were washed and incubated with nonblocking mouse monoclonal anti-VEGF antibody, 2C3 (Brekken et al., 1998), or rabbit polyclonal anti-gelonin IgG. For competition studies of VEGF121/rGel and VEGF121, binding of the VEGF121/rGel fusion protein was detected by using a rabbit anti-gelonin antibody. Mouse and rabbit IgG were detected by HRP-labeled goat anti-mouse and anti-rabbit antibodies, respectively (Dako). Peroxidase activity was measured by adding O-phenylenediamine (0.5 mg/ml) and hydrogen peroxide (0.03% vol/vol) in citrate-phosphate buffer (pH 5.5). The reaction was stopped by the addition of 100 ml of 0.18 M of H2SO4. The absorbance was read at 490 nM. In competition experiments, a 10-fold molar excess of VEGF121 was premixed with VEGF121/rGel before addition to the plate.
As shown in
VEGF121/rGelonin and VEGF121-Induced Phosphorylation of KDR
Porcine aortic endothelial cells (PAE/KDR) overexpressing the kinase domain receptor (KDR) were incubated overnight in F-12 culture medium and then incubated at 37° C. for 5 min with 100 mM Na3 VO4. VEGF or VEGF121/rGel then were added and, at various times, cells were lysed by the addition of a lysis buffer (50 mM Hepes, pH 7.4/150 mM NaCl/1 mM EGTA/10 mM sodium pyrophosphate/1.5 mM MgCl2/100 mM NaF/10% (vol/vol) glycerol/1% Triton X-100). Cell lysates were centrifuged (16,000×g), the supernatants were removed, and their protein concentrations were determined. Lysate supernatants were incubated with 9 mg anti-phosphotyrosine monoclonal antibody (Santa Cruz Biotechnology) for 2 h at 4° C. and then precipitated by the addition of Protein A Sepharose beads for 2 h at 4° C. Beads were washed and mixed with SDS sample buffer, heated for 5 min at 100° C., centrifuged, analyzed by SDS/10% PAGE, and then transferred to nitrocellulose filters. The membranes were blocked with 5% nonfat dry milk and incubated with rabbit polyclonal anti-KDR antibody (1:250; Santa Cruz Biotechnology) for 1 h at room temperature. The membranes then were washed, incubated with a peroxidase-linked goat anti-rabbit antibody (1:2,000) for 1 h at room temperature, and then enhanced chemiluminescence reagent (Amersham Pharmacia) was used to visualize the immunoreactive bands.
Results from these experiments showed that addition of VEGF121/rGel or VEGF121 increased phosphotyrosine content. There were two phases of phosphorylation; an early phase (1-10 min) and a later phase (4-8 h). The time course of induction of KDR phosphorylation was the same for VEGF121/rGel and VEGF121. Phosphorylation of FLT-1 in PAE/FLT-1 cells treated with either VEGF121/rGel or VEGF121 was not observed, as expected from the weaker signaling of FLT-1 compared with KDR observed by others.
Although VEGF121/rGel induces phosphorylation of KDR receptor, no growth-stimulatory effects of the fusion toxin on VEGF receptor-expressing cells were observed. These findings are in keeping with studies of other fusion toxins such as IL-2/DT that initially stimulate target cells in a manner similar to that of IL-2 itself, but ultimately kill the target cells through the actions of the internalized toxin.
Cytotoxicity of VEGF121/rGelonin to Endothelial Cells In Vitro
To determine cytotoxicity on adult bovine aortic arch-derived endothelial cells (ABAE), log-phase adult bovine aortic arch-derived endothelial cells in DMEM [10% (vol/vol) FBS] were diluted to 4,000 cells per 200 ml. Aliquots (200 ml) were added to 96-well flat-bottomed tissue culture plates and incubated at 37° C. for 1-72 h in 5% CO2. Purified VEGF121/rGel or rGel were diluted in culture medium to various concentrations, added to the plate, and the cultures were incubated for 72 h. Remaining adherent cells were stained by the addition of 100 ml of crystal violet [0.5% in 20% (vol/vol) methanol]. Dye-stained cells were solubilized by the addition of 100 ml of Sorenson's buffer [0.1M sodium citrate, pH 4.2 in 50% (vol/vol) ethanol]. The absorbance was measured at 595 nM.
To determine cytotoxicity on mouse brain-derived endothelial cells bEnd.3, the cells were seeded at a density of 50,000/well in 24-well plates. Twenty-four hours later, VEGF121/rGel or rGel alone were added at various concentrations. After 5 days of treatment at 37° C., remaining attached cells were trypsinized and counted. The results are presented as total cell number per well. Two identical experiments were performed in duplicate. Standard error in all experiments was less than 5% of the mean.
To determine cytotoxicity on PAE/KDR and PAE/FLT-1 cells, log-phase PAE/KDR cells and PAE/FLT-1 cells in F-12 medium [10% (vol/vol) FBS] were diluted to 3,000 cells per 200 ml. Aliquots (200 ml) were added to 96-well flat-bottomed tissue culture plates and incubated at 37° C. for 24 h in 5% CO2. Purified VEGF121/rGel or rGel were diluted in culture medium, added to the plate, and incubated for 72 h. Adherent cells were quantified by using the crystal violet staining method described above.
VEGF121/rGel was specifically toxic to KDR/Flk-1 expressing endothelial cells in vitro (
The ratio of IC50 values of rGel to VEGF121/rGel was calculated for each cell type. This ratio (the targeting index) represents the ability of the VEGF component of the fusion construct to mediate the delivery of the toxin to the endothelial cell surface and into the intracellular ribosomal compartment. As summarized in Table 1, bEnd.3 and adult bovine aortic arch-derived endothelial cells were, respectively, 100-fold and 9-fold more sensitive to the fusion construct than they were to free rGel.
2 × 105
Selective Cytotoxicity of VEGF121/rGelonin for Dividing PAE/KDR Cells
VEGF121/rGel was 60-fold more toxic to PAE/KDR cells in log-phase growth than it was to PAE/KDR cells that had been grown to confluence and rested (Table 1). This effect was not caused by differences in KDR expression, because the cells expressed the same number of KDR receptors per cell in both phases of growth. The log-phase PAE/KDR cells also were more sensitive to rGel itself than were the confluent cells, suggesting that the quiescence of confluent cells impacts their sensitivity to both targeted and nontargeted rGel. It is possible that the rate or route of entry of both VEGF121/rGel and rGel is different for dividing and nondividing cells.
VEGF121/rGelonin Binds to Both KDR and FLT-1
VEGF121 has been shown to bind to the FLT-1 receptor with greater affinity than to KDR. Because cytotoxicity of VEGF121/rGel to KDR-expressing cells was found to be nearly 600-fold greating than for FLT-1 expressing cells, the relative binding of VEGF121/rGel to PAE cells expressing each of the receptors was investigated.
ELISA analysis was performed to confirm the expression of both receptors on the cell surface using receptor-specific antibodies (data not shown). Expression of VEGFR-1 (FLT-1) and VEGFR-2 (KDR) was confirmed by western blot (
In order to confirm that VEGF121/rGel bound to human VEGFR-1 and VEGFR-2 and that the presence of recombinant gelonin did not interfere with the binding properties of VEGF121 the binding of radiolabeled VEGF121/rGel to both KDR and FLT-1 receptors expressed on the surface of PAE cells was investigated. One hundred μg of VEGF121/rGel was radiolabeled with 1 mCi of NaI125 using Chloramine T27 for a specific activity of 602 Ci/mMol. Cells were grown overnight in 24-well plates. Non-specific binding sites were blocked for 30 minutes with PBS/0.2% gelatin followed by incubation for 4 hours with 125I-VEGF121/rGel in PBS/0.2% gelatin solution. For competition experiments, cold VEGF121/rGel or gelonin were pre-mixed with 125I-VEGF121/rGel. Cells were washed four times with PBS/0.2% gelatin solution, detached and bound cpm was measured.
Internalization of VEGF121/rGelonin into PAE/KDR Cells
The internalization of VEGF121/rGel into PAE/KDR and PAE/FLT-1 cells was investigated using immunofluorescence staining. PAE/KDR and PAE/FLT-1 cells were incubated with 4 μg/ml VEGF121/rGel at various time points. After stripping the cell surface, cells were fixed with 3.7% formaldehyde and permeabilized with 0.2% Triton X-100. Non-specific binding sites were blocked with 5% BSA in PBS. Cells were then incubated with a rabbit anti-gelonin polyclonal antibody (1:200) followed by a TRITC-conjugated anti-rabbit secondary antibody (1:80). Nuclei were stained with propidium iodide (1 μg/ml) in PBS. The slides were fixed with DABCO media, mounted and visualized under fluorescence (Nikon Eclipse TS1000) and confocal (Zeiss LSM 510) microscopes.
VEGF121/rGel was detected in PAE/KDR cells within 1 hour of treatment with the immunofluoresence signal progressively increasing to 24 hours (
Cytotoxic Effects of VEGF121/rGelonin as a Function of Exposure Time on Endothelial Cells
The IC50 of VEGF121/rGel incubated for 72 hours on log-phase PAE/KDR cells has been shown to be about 1 nM. However, VEGF121/rGel internalizes into these cells within one hour of incubation. To study the cytototoxic effect of VEGF121/rGel as a function of exposure time of this agent on endothelial cells, cells were incubated with VEGF121/rGel from 1-72 hours and its cytotoxicity on PAE/KDR cells was assessed at the end of the 72-hour period.
While VEGF121/rGel retained cytotoxicity even after a one hour incubation, appreciable cytotoxicity was observed after 24 hours and maximal cytotoxic effect of VEGF121/rGel on PAE/KDR cells was observed after 48 hours (
Cytotoxic Mechanism of VEGF121/rGelonin
In order to investigate the mechanism of cytotoxicity of VEGF121/rGel to PAE/KDR cells, a TUNEL assay was performed for 24, 48 and 72 hours. Log phase PAE/KDR and PAE/FLT-1 cells were diluted to 2000 cells/100 μl. Aliquots (100 μl) were added in 16-well chamber slides (Nalge Nunc International) and incubated overnight at 37° C. with 5% CO2. Purified VEGF121/rGel was diluted in culture media and added at 72, 48 and 24 hour time points at a final concentration of 1 nM (twice the IC50). The cells were then processed and analyzed for TUNEL as described by the manufacturer of the reagent. Positive control cells were incubated with 1 mg/ml DNAse for 10 minutes at 37° C.
No TUNEL staining was observed with PAE/KDR cells exposed to VEGF121/rGel up to 72 hours (
Effects of VEGF121/rGel on PARP-mediated apoptosis were investigated by pre-incubating PAE/KDR cells with 100 mM Na2VO4 for 5 minutes at 37° C. followed by stimulation with VEGF121/rGel or VEGF121 for 5 minutes, 30 minutes, 4 h, 24 h and 48 h. Cells were washed and lysed. Cell lysate was analyzed by Western using an anti-PARP antibody. Western blot analysis of these cells showed that VEGF121/rGel did not activate PARP-mediated apoptosis (
Inhibition of Tumor Growth In Vivo by VEGF121/rGelonin
Human melanoma xenograft model was established as follows. Female nu/nu mice were divided into groups of five mice each. Log-phase A-375M human melanoma cells were injected s.c. (5×106 cells per mouse) into the right flank. After the tumors had become established (˜50 mm3), the mice were injected with VEGF121/rGel through a tail vein five times over an 11 day period. The total dose of VEGF121/rGel was 17 or 25 mg/kg. Other mice received rGel alone at a dose totaling 10 mg/kg. Mice were killed by cervical dislocation after the 40th day of tumor measurement.
Human prostate cancer xenograft model was established as follows. Male nude mice weighing ˜20 g were divided into groups of five mice each. Log-phase, PC-3 human prostate tumor cells were injected s.c. (5×106 cells per mouse) in the right flank. The mice were injected with VEGF121/rGel through a tail vein every 2-3 days for 11 days. The total dose of VEGF121/rGel was 20 mg/kg. Other mice received rGel alone at a dose totaling 10 mg/kg. Tumor volume was calculated according to the formula: volume=L×W×H, where L=length, W=width, H=height.
As shown in
Human prostatic carcinoma (PC-3) tumors increased 12-fold in volume during the 26-day observation period (
Localization of VEGF121/rGelonin to Vascular Endothelium in Prostate Tumor Xenografts
Mice (three mice per group) bearing PC-3 human prostate tumors were injected intravenously with 50 ug of the fusion protein gelonin (2.5 mg/kg) or free gelonin (1 mg/kg). The mean tumor volume per group was 260 mm3. Thirty minutes later, mice were killed, exsanguinated, and all major tissues were snap frozen. Frozen sections were cut and double stained with pan-endothelial marker MECA-32 (5 mg/ml) followed by detection of the localized fusion protein using rabbit anti-gelonin antibody (10 mg/ml). MECA-32 rat IgG was visualized with goat anti-rat IgG conjugated to FITC (red fluorescence). Anti-gelonin antibody was detected with goat anti-rabbit IgG conjugated to Cy-3 (green fluorescence). Colocalization of both markers was indicated by a yellow color. Anti-gelonin antibody had no reactivity with tissue sections from mice injected with saline or VEGF121. To determine the percentage of vessels with localized fusion protein, the number of vessels stained with MECA-32 (red), gelonin (green), or both (yellow) were counted at a magnification of ×200 in at least 10 fields per section. Two slides from each mouse were analyzed, and the average percentage of positive vessels was calculated.
As shown in
Destruction and Thrombosis of Tumor Vessels by VEGF121/rGelonin
Mice bearing s.c. PC-3 tumors were given one i.v. dose of VEGF121/rGel (2.5 mg/kg) or saline. The mice were killed 48 h later, and the tumors and various organs were removed. Paraffin sections were prepared and stained with hematoxylin and eosin. The tumors from VEGF121/rGel recipients (
Cytotoxicity of VEGF121/rGelonin to MDA-MB-231 Breast Tumor Cells
As assessed by Western blot, MDA-MB-231 breast cancer cells do not appear to express VEGFR-1 or VEGFR-2, the receptors which bind VEGF121 (
Localization of VEGF121/rGelonin to Vascular Endothelium in Breast Tumor Xenografts
SCID mice (3 mice per group) bearing orthotopic MDA-MB-231 tumors were intravenously injected with 50 ug of the fusion protein or equivalent amount of free gelonin. The mean tumor volume per group was 260 mm3. Four hours later the mice were sacrificed and exsanguinated. All major organs and tumor were harvested and snap-frozen for preparation of cryosections.
Frozen sections were double stained with a pan-endothelial marker MECA 32 (5 ug/ml) followed by detection of the localized fusion protein using rabbit anti-gelonin antibody (10 ug/ml). MECA 32 rat IgG (provided by Dr. E. Butcher of Stanford University, CA) was visualized by goat anti-rat IgG conjugated to FITC (green fluorescence). Rabbit anti-gelonin antibody was detected by goat anti-rabbit IgG conjugated to Cy-3 (red fluorescence).
Co-localization of both markers was indicated by yellow color. Anti-gelonin antibody had no reactivity with tissues sections derived from mice injected with saline or with VEGF121. To determine % of vessels with localized fusion protein, MECA 32 positive, gelonin-positive and vessels with combined color were counted at magnification of ×200 in at least 10 fields per section. Two slides from each mouse were analyzed and percent of positive vessels was averaged.
As shown in
The following examples utilize a breast cancer pulmonary metastatic model to establish VEGF121/rGel fusion toxin can inhibit metastatic spread and vascularization of metastases.
Human breast carcinoma MDA-MB-231 cells consistently lodge in lungs following intravenous injection into the tail vein of athymic or SCID mice. Micrometastases are first detected 3 to 7 days after injection of 5×105 cells and macroscopic colonies develop in 100% of the injected mice within 4 to 7 weeks. Mortality occurs in all mice within 10-15 weeks. This model of experimental breast cancer metastasis examines the ability of tumor cells to survive in the blood circulation, extravasate through the pulmonary vasculature and establish growing colonies in the lung parenchyma.
Female SCID mice, aged 4-5 weeks, were injected in a tail vein with 0.1 ml of MDA-MB-231 cell suspension (5×105 cells). The mice were randomly separated into two groups (6 mice per group) and were treated with either VEGF121/rGel or gelonin alone (100 μg intraperitoneally, 6 times total with an interval of 3 days) starting the 8th day after the injection of cells. Treatment with VEGF121/rGel for 2 weeks allow the mice to receive the maximal tolerated accumulative dose of the drug (600 μg per mouse). Prior studies established that VEGF121/rGel given at such dose did not cause histopathological changes in normal organs. The accumulative dose of 640-800 μg of total VEGF121/rGel fusion protein, given i.p. over period of 4 weeks, did not induce significant toxicity as judged by morphological evaluation of normal organs. Transient loss of weight (˜10%) was observed 24 hours after most of the treatments with complete weight recovery thereafter.
Metastatic colonies were allowed to expand for three weeks after treatment with VEGF121/rGel in order to evaluate long-term effect of VEGF121/rGel on the size of the colonies, proliferation index of tumor cells and their ability to induce new blood vessel formation. Three weeks after termination of the treatment, the animals were sacrificed and their lungs were removed. One lobe was fixed in Bouin's fixative and the other lobe was snap-frozen. After fixation in Bouin's fixative, the tumor colonies on the lung surface appear white, whereas the normal lung tissue appears brown. The number of tumor colonies on the surface of each lung was counted and the weight of each lung was measured. The values obtained from individual mice in the VEGF121/rGel and rGel groups were averaged per group.
Effects of VEGF121/rGelonin on the Number, Size And Vascular Density of MDA-MB-231 Pulmonary Metastatic Foci
Frozen samples of lung tissue was cut to produce sections of 6 μm. Blood vessels were visualized by MECA 32 antibody and metastatic lesions were identified by morphology and by 6w/32 antibody directed against human HLA antigens. Hybridoma producing the mouse monoclonal 6w/32 antibody was purchased from ATCC. The 6w/32 antibody was purified from hybridoma supernatant using Protein A resin.
Each section was double stained by MECA 32 and 6w/32 antibodies to ensure that the analyzed blood vessels are located within a metastatic lesion. Slides were first viewed at low magnification (×2 objective) to determine total number of foci per a cross-section. Six slides derived from individual mice in each group were analyzed and the number was averaged. Images of each colony were taken using digital camera (CoolSnap) at magnifications of ×40 and ×100 and analyzed using Metaview software that allows measurements of smallest and largest diameter, perimeter (μm) and area (mm2).
The vascular endothelial structures identified within a lesion were counted and number of vessels per each lesion was determined and normalized per mm2. The mean number of vessels per mm2 was calculated per each slide and averaged per VEGF121/rGel and rGel groups (6 slides per group). The results are expressed±SEM. The same method applied to determine the mean number of vessels in non-malignant tissues.
Treatment with VEGF121/rGel but not with free gelonin significantly reduced both the number of colonies per lung and the size of the metastatic foci present in lung by 42-58% as shown in
The overall mean vascular density of lung colonies was reduced by 51% compared to the rGel treated controls (Table 3 and
aMice with MDA-MB-231 pulmonary micrometastases were treated i.p. with VEGF121/rGel or free gelonin as described.
bP value was calculated using t-Student test.
cLungs were fixed with Bouin's fixative for 24 hours. Number of surface white colonies was determined for each sample and averaged among 6 mice from VEGF121/rGel or rGel control group. Mean number per group ± SEM is shown. Numbers in parentheses represent range of colonies in each group.
dFrozen sections were prepared from metastatic lungs. Sections were stained with 6w/32 antibody recognizing human tumor cells. Number of intraparenchymal colonies identified by brown color was determined for each cross-section and averaged among 6 samples of individual mice from VEGF121/rGel or rGel control group. Mean number per group ± SEM is shown. Numbers in parentheses represent range of colonies in each group.
eArea of foci identified by 6w/32 antibody was measured by using Metaview software. Total number of evaluated colonies was 101 and 79 for rGel and VEGF121/rGel group, respectively. Six individual slides per each group were analyzed. The mean area of colony in each group ± SEM is shown.
fThe sum of all regions occupied by tumor cells and the total area of each lung cross-section was determined and % of metastatic regions from total was calculated. The values obtained from each slide were averaged among 6 samples from VEGF121/rGel or rGel control group. The mean % area occupied by metastases from total area per group ± SEM is shown.
aColonies identified on each slide of a metastatic lung were subdivided into 5 groups according to their largest diameter.
bFrozen lung sections from VEGF121/rGel or rGel treated mice were stained with MECA 32 antibody. A colony was defined as vascularized if at least one blood vessel branched out from the periphery and reached a center of the lesion. Six slides per each group derived from individual mice were analyzed and data were combined.
cTotal number of the analyzed colonies was 127 and 92 for rGel and VEGF121/rGel treated groups, respectively. Seventy percent of foci in the VEGF121/rGel-treated group were avascular whereas only 40% of lesions from the control group did not have vessels within the metastatic foci.
Effect of VEGF121/rGelonin on the Number of Cycling Cells in the MDA-MB-231 Pulmonary Metastatic Foci
Frozen sections of normal mouse organs and metastatic lungs were fixed with acetone for 5 min and rehydrated with PBST for 10 min. All dilutions of antibodies were prepared in PBST containing 0.2% BSA. Primary antibodies were detected by appropriate anti-mouse, anti-rat or anti-rabbit HRP conjugates (Daco, Carpinteria, Calif.). HRP activity was detected by developing with DAB substrate (Research Genetics).
To determine the number of cycling cells, tissue sections were stained with the ki-67 antibody (Abcam, Inc., Cambridge, UK) followed by anti-mouse IgG HRP conjugate. Sections were analyzed at magnification of ×100. Number of cells positive for ki-67 was normalized per mm2. The mean number±SD per VEGF121/rGel or control group is presented. The average numbers derived from analysis of each slide were combined per either VEGF121/rGel or rGel group and analyzed for statistical differences.
The number of cycling tumor cells in lesions from the VEGF121/rGel group was reduced by ˜60% as compared to controls (
Effect of VEGF121/rGelonin on flk-1 Expression in Tumor Vessel Endotheluim of MDA-MB-231 Pulmonary Metastatic Foci
The expression of VEGF receptor-2 on the vasculature of breast tumors metastatic to lung was assessed using the RAF-1 antibody. Frozen sections of lungs from mice treated with VEGF121/rGel or free gelonin were stained with monoclonal rat anti-mouse VEGFR-2 antibody RAFL-1 (10 μg/ml). RAFL-1 antibody was detected by goat anti-rat IgG-HRP. The expression of KDR on the remaining few vessels present in lung metastatic foci demonstrated a significant decline compared to that of lung foci present in control tumors (
Summary of the Biological Properties of VEGF121/rGelonin
VEGF121/rGel was found to be selectively toxic to dividing endothelial cells overexpressing the KDR/Flk-1 receptor. Nondividing (confluent) endothelial cells were almost 60-fold more resistant than were dividing cells to the fusion construct and also were more resistant to free gelonin (Table 1). These findings accord with those of previous studies that showed conjugates of vascular endothelial growth factor and diphtheria toxin were highly toxic to log-phase cells but were not toxic to confluent endothelial cells. The greater sensitivity of dividing endothelial cells to VEGF-toxin constructs may be because of differences in intracellular routing or catabolism of the construct as observed with other targeted therapeutic agents.
Cytotoxicity studies demonstrated that expression of the KDR/Flk-1 receptor is needed for VEGF121/rGel to be cytotoxic. Cells overexpressing KDR/Flk-1 (>1×105 sites per cell) were highly sensitive to the VEGF121/rGel fusion construct, whereas cells expressing fewer than 0.4×105 sites per cell were no more sensitive to the fusion toxin than they were to free gelonin. Again, the requirement to surpass a threshold level of KDR/Flk-1 for cytotoxicity may contribute to the safety of VEGF121/rGel. In normal organs, including the kidney glomerulus and pulmonary vascular endothelium, the level of KDR/Flk-1 may be below that needed to cause toxicity. The number of receptors for vascular endothelial growth factor on endothelial cells in the vasculature of normal organs has been reported to be significantly lower than on tumor vasculature. Indeed, one could not detect binding of VEGF121/rGel to normal vascular endothelium in organs other than the kidney, where weak binding was observed. Furthermore, no damage to vascular endothelium was observed in normal organs, including the kidney.
Other gelonin-based-targeted therapeutics also have been observed to become toxic to cells only when a certain threshold level of binding is surpassed. In a recent study of immunotoxins directed against the c-erb-2/HER2/neu oncogene product, immunotoxins were not cytotoxic to tumor cells expressing less than about 1×106 HER2/neu sites per cell. The lack of sensitivity of cells having low levels of receptors is presumably because the cells internalize too little of the toxin or traffic it to compartments that do not permit translocation of the toxin to the ribosomal compartment.
Although VEGF/rGel fusion can bind to both the KDR and FLT-1 receptors, only cells expressing KDR were able to internalize the construct thereby delivering the toxin component to the cytoplasmic compartment. It has been suggested that it is the interaction of vascular endothelial growth factor with the KDR receptor but not the FLT-1 receptor that is responsible for the growth proliferative signal on endothelial cells. Other studies suggest that the KDR receptor is primarily responsible for mediating the vascular permeability effects of VEGF-A. Although FLT-1 receptor may modulate signaling of the KDR receptor and impact monocyte response to vascular endothelial growth factor, its role in neovascularization has not been well-defined.
The presence of FLT-1, even at high levels, does not seem to mediate cellular toxicity of the VEGF121/rGel fusion toxin. Although VEGF binds to the FLT-1 receptor, the current study has been unable to demonstrate receptor phosphorylation as a result of ligand binding. It has been suggested that receptor phosphorylation may be required for KDR signaling and internalization. If so, the receptor-fusion-toxin complex may not internalize efficiently after binding to FLT-1 for the fusion protein to be routed to an intracellular compartment from which the toxin can escape to the cytosol. The relative contributions of the FLT-1 and KDR receptors to the biological effects of vascular endothelial growth factor examined by using a monoclonal antibody that blocks the interaction of vascular endothelial growth factor with KDR/Flk-1 but not FLT-1 demonstrate that KDR/Flk-1 is the major receptor determining the vascular permeability-inducing and angiogenic effects of vascular endothelial growth factor in tumors.
Another important observation was that the cytotoxic effects of the VEGF121/rGel construct on vascular endothelial cells did not involve an apoptotic mechanism. This is in sharp contrast to studies of other toxins such as ricin A chain (RTA) and Pseudomonas exotoxin (PE) which demonstrate generation of apoptotic effects that are mediated, at least in part, by caspase activation. It has been suggested that PE toxins may generate cytotoxic effects through both caspase-dependant and protein synthesis inhibitory mechanisms. Despite the sequence homology of ricin A chain and rGel and the known similarities in their mechanism of action, it appears that these two toxins differ in their pro-apoptotic effects. One possible explanation for the observed differences in apoptotic effects between ricin A chain and the rGel toxin could be in the cell types examined. The cells targeted in the current study of rGel are non-transformed endothelial cells while those in the ricin A chain study were tumor cells.
The exposure duration studies for the VEGF121/rGel fusion toxin demonstrate that as little as 1 hr exposure to target cells is required to develop a cytotoxic effect 72 hrs later. However, continual exposure for up to 48 hrs was shown to improve the cytotoxic effect by almost 10 fold. Should pharmacokinetic studies demonstrate a relatively short plasma half-life for this agent, this may suggest that optimal therapeutic effect could be achieved by maintaining blood concentrations of drug at therapeutic concentrations for at least 48 hrs. This could be achieved by frequent interval dosing or continuous infusion but may be important in the development of pre-clinical and clinical dosing strategies.
The antitumor effects of the VEGF121/rGel fusion construct against both melanoma and human prostate carcinoma xenografts was impressive in magnitude and prolonged. A-375M and PC-3 cells in culture were resistant to the fusion construct in vitro, despite the reported presence of KDR on the melanoma (but not on PC-3) cells. Therefore, the antitumor effects observed in vivo appear not to be caused by direct cytotoxic effects of VEGF121/rGel on the tumor cells themselves. The antitumor effect seems to be exerted indirectly on the tumor cells through specific damage to tumor vasculature. The VEGF121 fusion toxin localized to tumor blood vessels after i.v. administration. Vascular damage and thrombosis of tumor blood vessels were observed within 48 h of administration of VEGF121/rGel to PC-3 mice, consistent with the primary action of the construct being exerted on tumor vascular endothelium.
VEGF121/rGel also has an impressive inhibitory effect on tumor metastases. Administration of the VEGF121/rGel construct to mice previously injected (i.v.) with the MDA-MB-231 human breast tumor cells dramatically reduced the number of tumor colonies found in lung, their size and their vascularity. In addition, the number of cycling breast tumor cells within lung metastatic foci was found to be reduced by an average of 60%. In addition to the reduced number of blood vessels present in lung metastases of treated mice, the few vessels present had a greatly reduced expression of VEGFR-2. Therefore, VEGF121/rGel demonstrated an impressive, long-term impact on the growth and development of breast tumor metastatic foci found in lung.
The salient finding of the effects of VEGF121/rGel construct is that this fusion toxin is specifically cytotoxic to cells over-expressing the KDR receptor for VEGF. However, the human breast MDA-MB-231 cancer cells employed for the metastatic studies described above do not express this receptor and, therefore, were not directly affected by this agent. The antitumor effects of VEGF121/rGel observed on the MDA-MB-231 metastases thus appear to be solely the result of targeting tumor vasculature.
Neovascularization is a particularly important hallmark of breast tumor growth and metastatic spread. The growth factor VEGF-A and the receptor KDR have both been implicated in highly metastatic breast cancer. It is of interest to note that administration of VEGF121/rGel resulted in a 3-fold decrease in the number of Ki-67 labeled (cycling) cells in the metastatic foci present in lung (
The vascular-ablative effects of the VEGF121/rGel fusion construct alone were able to partially eradicate lung metastases. Although development of small, avascular, metastatic foci within lung tissue was observed, the growth of larger pulmonary metastases was completely inhibited by treatment with the VEGF121/rGel fusion toxin. It is conceivable that combination of VEGF121/rGel fusion construct with chemotherapeutic agents or with radiotherapeutic agents that directly damage tumor cells themselves may provide for greater therapeutic effect. Studies of several vascular targeting agents in combination with chemotherapeutic agents have already demonstrated a distinct in vivo anti-tumor advantage of this combination modality against experimental tumors in mice (Siemann et al., 2002). Studies by Pedley et al. (2002) have also suggested that combination of vascular targeting and radioimmunotherapy may also present a potent antitumor combination. Finally, studies combining hyperthermia and radiotherapy with vascular targeting agents have demonstrated enhanced activity against mammary carcinoma tumors in mice (Murata et al., 2001).
Treatment of Orthotopic BladderTumors With VEGF121/rGelonin
Direct cytotoxic effect of VEGF121/rGel and rGel on the highly tumorigenic and metastatic human bladder tumor cell line 253J B-V was initially evaluated in vitro and compared to the cytotoxic effect on PAE/KDR cells. Treatment of log-phase cells with VEGF121/rGel for 72 h showed the greatest cytotoxic effect against PAE/KDR cells, with an IC50 of 1 nM (
The therapeutic and anti-angiogenic effect of the fusion protein VEGF121/rGel was evaluated against human bladder cancer xenografts growing in athymic nude mice. Each mouse was anesthetized with sodium pentobarbital (25 mg/kg) i.p. and placed in the supine position. A lower midline incision was performed, and the bladder was exposed. The highly tumorigenic and metastatic 253J B-V human transitional cell carcinoma cells (3.5×105 cells in 50 μl of HBSS) were implanted into the wall of the bladder in the area of the bladder dome using 30-gauge needles on disposable 1 ml syringes. A successful implantation was indicated by a bleb in the bladder wall serosa. The abdominal wound was closed in one layer with metal wound clips.
Thirty mice were randomized into three treatment groups, and treatment began on the third day after tumor injection into the bladder. The animals were treated with the following protocol: Group 1, 200 μl saline every other day for ten days (5 treatments); Group 2, 29 μg recombinant gelonin in 200 μl saline every other day for ten days (5 treatments); Group 3, 80 μg VEGF121/rGel in 200 μl saline every other day for ten days (5 treatments). Twenty-one days after tumor injection, the animals were sacrificed and the bladders were harvested, weighed and processed.
As shown in
Bladder tumors from treated mice were processed for histology and immunohistochemical analysis. Immunofluorescence of tumor tissue sections with anti-CD-31 and anti-gelonin antibodies showed dramatic co-localization of VEGF121/rGel with CD-31 on tumor neovasculature (
To study the in vivo effect on tumor cells as a result of VEGF121/rGel cytotoxicity on endothelial cells, bladder tumors from mice treated with VEGF121/rGel, rGel or saline were stained for apoptotic effects. Both necrotic as well as non-necrotic regions were examined by immunofluorescent terminal deoxynucleotidyl-dUTP nick-end labeling (TUNEL) assay. As shown in
Laser Scanning Cytometry (LSC)-mediated quantitative analysis was used to determine the number of TUNEL positive cells in each tissue section. Negative control slides were used to set the gates on the scattergram, and each bladder tumor section was scanned by LSC to determine the percentage of apoptotic cells in 1×104 total cells per tumor. Tumor sections from rGel-treated mice had 2.73±0.72% (n=3) TUNEL positive cells, whereas tumor sections from VEGF121/rGel-treated mice had 6.3±1.67% (n=3) TUNEL positive cells (p=0.027). Thus, VEGF121/rGel is a cytotoxic agent that targets the neovasculature of bladder carcinoma and a useful combination therapy for the treatment of bladder cancer.
VEGF121/rGelonin Inhibits Intrafemoral PC3 Tumor Growth and Reduces the Number of Osteoclasts
The anti-tumor effect of the fusion protein VEGF121/rGel was evaluated in a prostate cancer bone model by injecting PC3 tumor cells into the distal epiphysis of the right femur of athymic nude mice. The animals were anesthetized with intramuscular injections of ketamine (100 mg/kg) plus acepromazine (2.5 mg/kg). Aliquots of 5×104 of PC3 cells were diluted in 5 μl of growth medium and then injected into the distal epiphysis of the right femur of each mouse using a 28-gauge Hamilton needle. The contralateral femur was used as an internal control. Twenty mice were randomized into two treatment groups. Treatment began one week after tumor placement. The animals were treated (i.v.) with the following protocol: Group 1, 200 μl saline every other day for nine days (5 treatments); Group 2, 180 μg VEGF121/rGel in 200 μl saline every other day for nine days (5 treatments). Mice were monitored weekly for tumor bulk and bone loss. Tumor growth was monitored by X-ray analysis and animals with large osteolytic lesions or bone lysis were sacrificed.
Prostate cancer-bearing mice treated with saline developed osteolytic lesions (FIGS. 25) and 50% survival occurred 40 days after tumor placement (
TRAP staining of bone sections revealed a dramatic increase in the number of osteoclasts in the tumor-bearing leg of mice treated with saline (
VEGF121/rGelonin is Cytotoxic to Osteoclast Precursor Cells and Inhibits Differentiation to Mature Osteoclasts
To examine the effect of VEGF121/rGel in the bone microenvironment and test if VEGF121/rGel may be targeting osteoclast precursor cells in vivo, the effect of VEGF121/rGel fusion toxin on RANKL-induced osteoclast differentiation of osteoclast precursor RAW cells was examined in vitro. The effect of VEGF121/rGel and rGel on M-CSF and RANKL-dependent osteoclast differentiation of primary bone marrow monocytes was also examined.
M-CSF dependent, non-adherent bone marrow cells representing cells of the monocyte lineage were isolated from tibiae and femora of mice. Tibiae and femora were aseptically dissected from mice. Bone ends were cut off, and marrow was forced out in MEM supplemented with 10% FBS and penicillin. The marrow suspension was filtered through a fine meshed sieve to remove bone particles and gentle pipetting was used to obtain a single cell suspension. The bone marrow cells were washed and plated at 1.5−2×107 cells/10 cm dish with 10 ml of MEM and cultured for 24 h in the presence of M-CSF (10 ng/ml). On the following day, non-adherent cells were re-suspended in MEM, plated at 2.5×104 cells per well in a 96 well dish for cytotoxicity assays or 5×103 per well in a 96 well plate for osteoclast assays. The cells were then cultured for 3 days in the presence of 10 ng/ml M-CSF before they were used for further experiments.
For in vitro osteoclast differentiation assay, primary bone marrow monocytes or RAW 264.7 cells were cultured in 96-well dishes at a density of 5×103 cells per well and 3×103 cells per well, respectively. RAW 264.7 cells were cultured with 100 ng/ml RANKL. Primary bone marrow monocytes were cultured with 10 ng/ml M-CSF and 100 ng/ml RANKL and culture medium was changed on day 3. Osteoclast differentiation was determined by counting the total number of multinucleated (3 nuclei), tartrate-resistant acid phosphatase (TRAP)-positive cells per well on day 5 using Leucocyte Acid phosphatase kit (Sigma-Aldrich, St. Louis, Mo.).
As shown in
Similar to the effects on RAW cells, VEGF121/rGel inhibited M-CSF and RANKL-mediated osteoclast differentiation of primary mouse bone marrow-derived osteoclast progenitors in a dose-dependent manner (
Localization of VEGF121/rGelonin into Osteoclast Precursor Cells is Mediated by Flt-1
Because VEGF121/rGel exhibited targeted cytotoxicity on RAW and bone marrow-derived monocytes, the levels of expression of VEGF121 receptors Flk-1/KDR and Flt-1 were examined in these cells. PCR analysis indicated low levels of Flt-1, but no Flk-1/KDR transcript, in RAW cells (
PCR analysis of VEGF-A isoforms indicated the presence of low levels of VEGF164 and VEGF120. VEGF189 and VEGFx were not detected. Stimulation of RANKL-mediated osteoclastogenesis did not change the levels of Flk-1/KDR or VEGF-A isoforms, but downregulated Flt-1 transcript by 72 h after addition of RANKL (
Based on the observation that the cytotoxicity of VEGF121/rGel on endothelial cells is mediated through Flk-1/KDR and not Flt-1, it is hypothesized that Flk-1/KDR plays an important but as yet unknown role in RANKL-mediated osteoclastogenesis. However, it is also possible that the biology of VEGF receptors is different in osteoclasts compared to endothelial cells, and VEGF121/rGel is able to inhibit formation of osteoclasts via Flt-1. To this end, whether VEGF121/rGel was delivered into the cytoplasm of the cells was examined by immunostaining.
To study internalization of VEGF121/rGel into RAW cells, the cells were incubated with various concentrations of VEGF121/rGel or rGel for various periods of time. To demonstrate receptor specificity, the cells were pre-treated with Flt-1 or Flk-1 neutralizing antibodies for one hour prior to treatment with VEGF121/rGel or rGel. Glycine buffer (500 mM NaCl, 0.1 glycine, pH 2.5) was used to strip the cell surface of non-internalized VEGF121/rGel. Cells were fixed with 3.7% formaldehyde and permeabilized with 0.2% Triton X-100. Non-specific binding sites were blocked with 5% BSA in PBS. The cells were then incubated with a rabbit anti-gelonin polyclonal antibody (1:200) followed by a TRITC-conjugated anti-rabbit secondary antibody (1:80). Nuclei were stained with propidium iodide (1 μg/ml) in PBS. The slides were fixed with DABCO media, mounted and visualized under fluorescence (Nikon Eclipse TS1000) and confocal (Zeiss LSM 510) microscopes.
As shown in
To determine the role of VEGF121 receptors in VEGF121/rGel-mediated cytotoxicity of osteoclast precursor cells, bone marrow-derived monocytes were preincubated with neutralizing antibodies to Flt-1 or Flk-1/KDR for one hour prior to addition of VEGF121/rGel for 72 h. Cell viability was not affected by the addition of up to 20 μg/ml anti-Flk-1 antibody (
The following examples describe a fusion construct of VEGF121 and proapoptotic enzyme granzyme B (GrB) designed for specific delivery to tumor neovasculature. Human granzyme B gene was cloned from human cutaneous T-cell lymphoma (HuT-78) cells and then fused to VEGF121 via a short, flexible tether using a PCR-based construction method. The fusion protein was expressed in Escherichia coli and purified by nickel-NTA metal affinity chromatography. The fusion protein GrB/VEGF121 was characterized and the biological activities and mechanism were determined.
RNA from HuT-78 cells was isolated and target premature human granzyme B cDNA was amplified by reverse transcription-PCR using the following primers: Ncolgb, 5′-GGTGGCGGTGGCTCCATGGAACCAATCCTGCTTCTG-3′ (SEQ ID NO:5) and CxhoIgb, 5′-GCCACCGCCTCCCTCGAGCTATTAGTAGCGTTTCATGGT-3′ (SEQ ID NO:6). The human granzyme B sequence with signal sequence was designated as premature granzyme B (˜800 bp) (
In cytotoxic cells, active granzyme B was generated from a zymogen by dipeptidyl peptidase I-mediated proteolysis, which removes the two residue (Gly-Glu) propeptide and exposes Ile21. The amino-terminal Ile-Ile-Gly-Gly sequence of granzyme B is necessary for the mature, active granzyme B.
To construct GrB/VEGF121 fusion gene, the coding sequence of granzyme B was amplified by PCR from Ile21, effectively deleting the signal sequence and Gly-Glu domain. At the same time, a cleavage site for EK (DDDDK, SEQ ID NO:7) was inserted upstream and adjacent to Ile21. Mature granzyme B was attached to the recombinant VEGF121 carrier via flexible tether (G4S). The fused gene fragment was then introduced into the XbaI and XhoI sites of the pET32a(+) to form the expression vector pET32GrB/VEGF121 (
The GrB/VEGF121 fusion gene was constructed by an overlap PCR method. Briefly, granzyme B coding sequence was amplified from gbTA-2 using the following primers: NgbEK, 5′-GGTACCGACGACGACGACAAGATCATCGGGGGACATG AG-3′ (SEQ ID NO:8) and Cgb, 5′-GGAGCCACCGCCACCGTAGCGTTTCATGGT-3′ (SEQ ID NO:9). These were designed to delete the signal sequence of premature granzyme B, insert an EK cleavage site at the amino terminus, and add a G4S linker sequence to the carboxyl terminus to serve as a link to the VEGF121 gene. VEGF121 sequence was amplified from a plasmid pET22-VEGF121 (from Dr. Philip Thorpe, University of Texas Southwestern Medical Center, Dallas, Tex.) using the following primers: Nvegf, 5′-GGTGGCGGTGGCTCCGCACCCATGGCAGAA-3′ (SEQ ID NO:10) and CxhoI veg, 5′-AAGGCTCGTGTCGACCTCGAGTCATTACCG CCTCGGCTTGTC-3′ (SEQ ID NO:11). To clone the fused genes into pET32a(+) vector with an EK site at the amino terminus of granzyme B, the fragment from pET32a(+) was amplified using the following primers: T7 promoter, 5′-TAATACGACTCACTATAG (SEQ ID NO:12) and CpET32EK, 5′-CTTGTCGTCGTCGTCGGTACCCAGATCTGG-3′ (SEQ ID NO:13). The primer has an EK site at carboxyl terminus overlapping with the amino terminus of the fused gene. Using overlap PCR, the fusion genes (EK-GrB/VEGF121) were constructed using as primers the T7 promoter and CxhoI veg. Amplified fragments were purified, digested with XbaI and XhoI, and cloned into pET32a(+) vector, designed as pET32GrB/VEGF121. A correct clone was chosen for transformation into AD494 (DE3) pLysS-competent cells for further induction and expression.
Bacterial colonies transformed with the constructed plasmid were grown in Luria broth medium (containing 400 mg/ml carbenicillin, 70 mg/ml chloramphenicol, and 15 mg/ml kanamycin) at 37° C. overnight at 240 rpm in a shaking incubator. The cultures were then diluted 1:100 in fresh Luria broth+antibiotics (200 mg/ml ampicillin, 70 mg/ml chloramphenicol, and 15 mg/ml kanamycin) and grown to A600nm=0.6 at 37° C.; thereafter, isopropyl-1-thio-b-D-galactopyranoside was added to a final concentration of 100 mM and the cells were incubated at 37° C. for 2 h to induce fusion protein expression. The cells were harvested, resuspended in 10 mM Tris (pH 8.0), and stored frozen at −80° C. for later purification.
Thawed, resuspended cells were lysed by addition of lysozyme to a final concentration of 100 mg/ml with agitation for 30 min at 4° C. followed by sonication. Extracts were centrifuged at 186,000×g for 1 h. The supernatant containing only soluble protein was adjusted to 40 mM Tris, 300 mM NaCl, and 5 mM imidazole (pH 8.0) and applied to nickel-NTA agarose resin equilibrated with the same buffer. The nickel-NTA agarose was washed with 300 mM NaCl and 20 mM imidazole and the bound proteins were eluted with 500 mM NaCl and 500 mM imidazole. Absorbance (280 nm) and SDS-PAGE analyses were performed to determine the presence of the polyhistidine-tagged protein, designated as Pro-GrB/VEGF121. The eluted Pro-GrB/VEGF121 was dialyzed against 20 mM Tris-HCl (pH 7.4) and 150 mM NaCl. The GrB moiety of Pro-GrB/VEGF121 was activated by the addition of bovine rEK to remove the polyhistidine tag according to the manufacturer's instructions (1 unit of rEK for cleavage of 50 mg protein incubated at room temperature for 16 h). The rEK was removed by EK capture agarose. The protein solution was then passed through a column containing Q-Sepharose to remove non-rEK-digested construct and nonspecific proteins. The product was analyzed by SDS-PAGE to determine purity, and Bio-Rad protein assay was used to determine protein concentration. Samples were then aliquoted and stored at 4° C.
One liter of the culture typically yielded ˜100 mg of the final purified GrB/VEGF121 product. SDS-PAGE analysis showed that the final purified GrB/VEGF121 fusion construct migrated under reducing conditions as a band at the expected molecular mass of 38 kDa (
Binding activity of GrB/VEGF121 was determined by ELISA. Ninety six-well plates coated with 50,000 cells/well of PAE/FLK-1, PAE/FLT-1, human melanoma A375M or human breast cancer SKBR3-HP cells were blocked by 5% BSA and then treated with purified GrB/VEGF121 at various concentrations. After washing, the plates were incubated with either GrB antibody or VEGF121 antibody followed by HRP-goat anti-mouse IgG. Then, the substrate 2,2′-azino-bis-3-ethylbenzthiazoline-6-sulfonic acid (ABTS) solution with 1 ml/ml of 30% H2O2 was added to the wells. Absorbance at 405 nm was measured after 30 min.
GrB/VEGF121 specifically bound to PAE/FLK-1 cells. However, the protein did not bind to PAE/FLT-1 cells or to melanoma A375M or human breast cancer SKBR3-HP cells, as detected by either an anti-GrB mouse monoclonal antibody (
Cells were plated in 16-well chamber slides (Nunc, Nalge Nunc International, Naperville, Ill.) at 1×104 cells/well and incubated overnight at 37° C. in a 5% CO2 air atmosphere. Cells were treated with 100 nM of GrB/VEGF121 for 4 h and then washed briefly with PBS. The cell surface was stripped by incubation with glycine buffer (500 mM NaCl, 0.1 M glycine [pH 2.5]) and neutralized for 2 min with 0.5 M Tris (pH 7.4) followed by wash with PBS. Cells were fixed in 3.7% formaldehyde for 15 min at room temperature, permeabilized for 10 min in PBS containing 0.2% Triton X-100 and washed thrice with PBS. Samples were incubated with 3% BSA for 1 h at room temperature to block nonspecific binding sites before incubating with anti-GrB mouse monoclonal antibody (1:100 dilution) at room temperature for 1 h followed by incubation with FITC-coupled anti-mouse IgG (1:100 dilution) at room temperature for 1 h. The walls and gaskets of the chamber slide were then removed carefully. After air drying, the slide was mounted and analyzed under a Nikon Eclipse TS-100 fluorescence microscope. Photographs were taken with a scope-mounted camera.
Immunofluorescent staining clearly showed that the GrB moiety of GrB/VEGF121 was delivered into the cytosol of PAE/FLK-1 but not into that of PAE/FLT-1 cells after treatment with GrB/VEGF121 for 4 h (
The cytotoxicity of GrB/VEGF121 was assessed against log-phase PAE/FLK-1 and PAE/FLT-1 cells in culture. PAE cells in Ham's F-12 medium with 10% fetal bovine serum were plated into 96-well plates at a density of 2.5×103 cells/well and allowed to adhere for 24 h at 37° C. in 5% CO2. After 24 h, the medium was replaced with medium containing different concentrations of GrB/VEGF121 or VEGF121/rGel. After 72 h, the effect of GrB/VEGF121 or VEGF121/rGel on the growth of cells in culture was determined using 2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-2H-tetrazolium-5-carboxanilide inner salt (XTT). Plates were read on a microplate ELISA reader at 540 nm.
An IC50 effect was found at a concentration of ˜10 nM on PAE/FLK-1 cells. However, no cytotoxic effects were found on PAE/FLT-1 cells at doses up to 200 nM (
The growth inhibitory effects of GrB/VEGF121 on the proliferation of PAE cells were evaluated by clonogenic assay. Briefly, 5×105 PAE cells/ml were incubated at 37° C. and 5% CO2 for 72 h with different concentrations of either GrB/VEGF121 or 100 nM of irrelevant fusion protein GrB/scFvMEL. Cells were then washed with PBS, trypsinized, counted by hemacytometer, and diluted serially. The serial cell suspensions were then plated in triplicate and cultured in six-well plates for 5-7 days. Cells were stained with crystal violet and colonies consisting of >20 cells were counted using an inverted light microscope. Growth inhibition was defined as the percentage of cell growth/number of colonies in treated samples in relation to that in the nontreated control sample.
In the clonogenic assay (
Cleavage of genomic DNA during apoptosis may yield double-stranded, low molecular mass DNA fragments as well as single-strand breaks (nicks) in high molecular mass DNA. The DNA strand breaks can be identified by labeling free 3′ hydroxyl termini with modified nucleotides in an enzymatic reaction. Cells (1×104 cells/well) were treated with GrB/VEGF121 at the IC50 concentration for different times (24 and 48 h) and washed briefly with PBS. Cells were fixed with 3.7% formaldehyde at room temperature for 20 min, rinsed with PBS, permeablized with 0.1% Triton X-100, 0.1% sodium citrate on ice for 2 min, and washed with PBS twice. Cells were incubated with TUNEL reaction mixture at 37° C. for 60 min followed by incubation with Converter-AP at 37° C. for 30 min and finally treated with Fast Red substrate solution at room temperature for 10 min. After the final wash step, the slides were mounted and analyzed for nucleus staining of apoptotic cells under a light microscope with 400× magnification.
TUNEL assay produced positive results on GrB/VEGF121-treated PAE/FLK-1 cells at 24 h (75%) and 48 h (85%) but not on GrB/VEGF121-treated PAE/FLT-1 cells (10%) (
PAE cells (5×107) were treated with GrB/VEGF121 at concentrations of 0.1 and 20 nM for 24 h. After cells were washed with 10 ml of ice-cold PBS, they were resuspended with 0.5 ml of 1× cytosol extraction buffer mix containing DTT and protease inhibitors and incubated on ice for 10 min. Cells were homogenized in an ice-cold glass homogenizer. The homogenate was centrifuged at 700×g for 10 min at 4° C. The supernatant was transferred to a fresh 1.5 ml tube and centrifuged at 10,000×g for 30 min at 4° C. The supernatant was collected and labeled as cytosolic fraction. The pellet was resuspended in 0.1 ml mitochondrial extraction buffer mix containing DTT and protease inhibitors, vortexed for 10 s, and saved as mitochondrial fraction. Protein concentrations were determined by using Bio-Rad Bradford protein assay. Aliquots of 30 mg from each cytosolic and mitochondrial fraction isolated from non-treated and treated cells were loaded on a 15% SDS-PAGE. Standard Western blot procedure was performed, and the blot was probed with mouse anti-cytochrome c antibody (1 mg/ml) or mouse anti-Bax antibody (1 mg/ml).
Western blot studies demonstrated that cytochrome c was released from mitochondria into the cytosol after treating PAE/FLK-1 cells with 20 nM GrB/VEGF121, but this effect was not observed on PAE/FLT-1 cells (
PAE cells were plated onto six-well plates (2×105 cells/well). Twenty-four hours later, cells were shifted to fresh culture medium containing 20 nM of GrB/VEGF121 (1.5 ml/well). After 24 h of incubation at 37° C., DNA was extracted and purified with DNA ladder kit (Roche) and fractionated on 1.5% agarose gels.
DNA laddering indicative of apoptosis was observed after a 24-h exposure with GrB/VEGF121 on PAE/FLK-1 cells. As expected, there was no DNA laddering detected on PAE/FLT-1 cells after treatment with the fusion construct (
PAE cells were treated with GrB/VEGF121, total cell lysates were loaded onto 12% SDS-PAGE, and standard Western blotting was performed. The results showed that treatment with GrB/VEGF121 cleaved caspase-8, caspase-3, and PARP in PAE/FLK-1 cells but not in PAE/FLT-1 cells (
Microarray Analysis of Human Umbilical Vein Endothelial Cells (HUVECs) Treated with VEGF121-rGel
To further elucidate the biochemical mechanisms that govern the effects of VEGF121/rGel on endothelial cells, HUVECs were treated with saline or the IC50 dose of VEGF121/rGel for 24 h. RNA was then isolated, evaluated for integrity, and subjected to microarray analysis
HUVEC RNA was amplified using protocol previously described. Test and control samples (HUVECs treated for 24 h with VEGF121/rGel or saline, respectively) were labeled using Cy3- and Cy5-dCTP in reverse transcription reaction. Duplicate experiments were conducted by dye swapping. The labeled samples were hybridized to a cDNA array of 2304 sequence-verified clones in duplicate printed by the Cancer Genomics Core Laboratory of the Department of Pathology at M. D. Anderson Cancer Center. The array included 4800 genes involved in signal transduction, stress response, cell cycle control, hypoxia, and metastatic spread. Hybridization was performed overnight at 60° C. in a humid incubator. After washing, the hybridized slides were scanned using a GENETAC LS IV laser scanner (Genomic Solutions, Ann Arbor, Mich.) and signal intensities were quantified with ARRAYVISION (Imaging Research Inc., St. Catherines, Ontario, Canada). Local background-subtracted spot intensities were used for further analysis. Differentially expressed genes were identified on the basis of a cutoff value of T value. Generally, a cutoff value of |3| is considered statistically significant.
Dye swapping experiments were designed to limit dye bias that raises concern in microarray experiments. The two factors addressed by this design are the differences in dye incorporation and gene-specific effects of the dye. Normalization of the data typically corrects for differences in incorporation of dye that affects all the genes. Dye-specific effects can be insignificant compared with other sources of variation in the experiment. Hence, the dye swapping experiments were treated as duplicates. The signal-to-noise ratio of the images was evaluated to determine the quality of the array. Only those spots with a signal-to-noise ratio of ≧2 were evaluated (80%). Genes that showed values greater than |2| in at least 3 of 4 arrays were identified, and the average fold change was determined.
On this basis, 22 genes (out of the 4800 in the microarray) were upregulated by VEGF121/rGel at 24 h (Table 4). In addition to upregulating select genes known to be induced by VEGF alone, treatment with VEGF121/rGel upregulated genes involved in inflammation, chemotaxis and transcription regulation.
Microarray data were verified by performing RT-PCR analysis on genes that showed the highest level of induction, namely E-selectin (SELE), cytokine A2 (SCYA2, MCP-1), tumor necrosis factor alpha induced protein 3 (TNFAIP3) and NF-kB inhibitor alpha (NF-kBla). Primers were designed on the basis of the accession numbers from the microarray and confirmation of homology using BLAST (NCBI). Induction of E-selectin in PAE/KDR cells was also verified by RT-PCR. GAPDH primers were used as controls. The primers used were as follows: SELE forward—5′GGTTTGGTGAGGTGTGCTC (SEQ ID NO:16); SELE reverse—5′TGATCTTTCCCGGAACTGC (SEQ ID NO:17); SCYA2 forward—5′ TCTGTGCCTGCTGCTCATAG (SEQ ID NO:18); SCYA2 reverse—5′ TGGAATCCTGAACCCACTTC (SEQ ID NO:19); TNFAIP3 forward—5′ATGCACCGATACACACTGGA (SEQ ID NO:20); TNFAIP3 reverse—5′ CGCCTTCCTCAGTACCAAGT (SEQ ID NO:21); NF-kBla forward—5′ AACCTGCAGCAGACTCCACT (SEQ ID NO:22); NF-kBla reverse 5′GACACGTGTGGCCATTGTAG (SEQ ID NO:23); porcine E-selectin (PORESEL) forward—5′GCCAACGTGTAAAGCTGTGA (SEQ ID NO:24); PORESEL reverse—5′ TCCTCACAGCTGAAGGCACA (SEQ ID NO:25); GAPDH forward—5′ GTCTTCACCACCATGGAG (SEQ ID NO:26); and GAPDH reverse—5′CCACCCTGTTGCTGTAGC (SEQ ID NO:27). Isolated RNA was subjected to first-strand cDNA synthesis as described by the manufacturer of the Superscript First Strand synthesis system (Invitrogen, Carlsbad, Calif.). RT-PCR was performed using a Minicycler PCR machine (MJ Research, Inc., San Francisco, Calif.).
When normalized for GAPDH, transcripts for E-selectin (SELE), cytokine A2 (SCYA2, MCP-1), tumor necrosis factor alpha induced protein 3 (TNFAIP3) and NF-kB inhibitor alpha (NF-kBla) were all increased after treatment with VEGF121/rGel, thus validating the results observed in the original microarray (
Because PAE/KDR cells have been used as in vitro models for endothelial cells in tumor neovasculature, the effect of VEGF121/rGel on gene induction and protein expression in these cells was investigated. PAE/KDR cells were treated with saline or the IC50 dose of VEGF121/rGel for up to 48 h. As shown in
The results suggest that treatment of HUVECs with VEGF121/rGel increases RNA levels of several genes that are involved in inflammation, chemotaxis, intermediary metabolism, and apoptotic pathways (Table I). A previous report showed that only two of these genes, MKP-1 and CXCR4, were upregulated after treatment with VEGF165 for 24 h. Therefore, for most of the genes found to be upregulated in the present study, the upregulation appears to be attributable to the VEGF121/rGel construct and not the VEGF component itself. This microarray analysis was the first performed on cells treated with a plant-derived protein toxin such as gelonin.
Of all the molecules we studied, the highest level of mRNA induced was that of the cell adhesion molecule E-selectin. In previous studies, treatment with VEGF induced adhesion molecules (E-selectin, VCAM-1, and ICAM-1) in HUVECs via an NF kB-mediated process. E-selectin has been shown to be upregulated after VEGF treatment or in response to inflammation and plays an important role in both tube formation and angiogenesis. Previous studies have shown that E-selectin also plays a major role in the adhesion of epithelial cancer cells to the endothelium and that the ability of cancer cell clones to bind E-selectin on endothelial cells is directly proportional to their metastatic potential. Moreover, drugs that inhibit the expression of E-selectin, such a s cimetidine, block the adhesion of tumor cells to the endothelium and prevent metastasis.
However, E-selectin does not necessarily have a role in the adhesion of all cancer cells, nor do all cancer cells require expression of the same endothelial adhesive molecule. The present study shows that VEGF121/rGel is a member of a class of molecules that can prevent E-selectin-mediated metastasis because protein levels barely doubled in both PAE/KDR and HUVECs after treatment with VEGF121/rGel. A similar pattern of induction of RNA but not protein levels was observed with other genes as well. For example, although MKP-1 RNA levels were induced in HUVECs after treatment with VEGF121/rGel, western blots of PAE/KDR and HUVEC whole cell extract did not show a corresponding increase in protein levels (data not shown). In addition, levels of ERK2, which was previously shown to be upregulated by MKP-1 in HUVECs after endothelial cell injury, did not show a change up to 48 h after VEGF121/rGel treatment. Taken together, we conclude VEGF121/rGel induces an increase in mRNA levels of genes that are important in cell adhesion, migration, and spread but generally does not induce a concomitant increase in protein expression. Since the rGel component of the fusion construct operates by inhibiting protein synthesis, VEGF121/rGel could inhibit synthesis of critical proteins that are important for suppression of these specific genes.
This data also suggest that in addition to exerting a cytotoxic effect, VEGF121/rGel may act through cellular mechanisms involved in inflammation and stress. Previous studies have showed that several genes are induced as a result of cellular inflammation. For example, early growth response factor 1 (EGR1), SCYA2, E-selectin and VCAM-1 are all up-regulated in HUVECs, and all of these genes are induced by treatment with VEGF121/rGel. In addition, several members of the small inducible cytokine (SCYA) family of proteins are overexpressed after VEGF121/rGel treatment. All of these SCYA proteins respond to inflammation stimuli and play a role in chemotaxis: SCYA2 plays a role in inflammation and wound healing; SCYA4 (MIP-1b) is involved in directional migration of cells during normal and inflammatory processes; and SCYA7 (MCP-3) and SCYA11 (eotaxin) share 65% amino acid sequence identity and play major roles in the recruitment and activation of eosinophils in allergic disorders. Another molecule that plays a role in chemotaxis is CXCR4. Although treatment with VEGF121/rGel increases the CXCR4 level to less than twice the level without treatment, array spot intensities and reproducibility data indicate that the increase is significant.
Transcription factors represent one of the larger classes of genes to be upregulated by treatment with VEGF121/rGel. Interestingly, two of them, NF-kBla (IkB-a) and NF-kB (p105 subunit), are from the NF-kB family. Since NF-kB and IkB-a interact in an autoregulatory mechanism, the upregulation of IkB-a is most likely due to NF-kB's mediating activation of the IkB-a gene, resulting in replenishment of the cytoplasmic pool of its own inhibitor. NF-kB may play a role in the upregulation of several genes, including SCYA2, SCYA7, SCYA11, and JunB. Another transcription factor, Kruppel-like factor (KLF4), has not been shown to be expressed in endothelial cells. However, this molecule is an important nuclear factor in the up-regulation of histidine decarboxylase, an enzyme that catalyzes the conversion of histidine to histamine, a bioamine that plays an important role in allergic responses, inflammation, neurotransmission, and gastric acid secretion.
Among the molecules governing apoptosis, TNFAIP3, a putative DNA binding protein in the NF-kB signal transduction pathway, functions by inhibiting NF-kB activation and TNF-mediated apoptosis. BIRC3, another gene that is upregulated by treatment with VEGF121/rGel, forms a heterodimer with a caspase-9 monomer in vitro and prevents the activation of caspase-9 in apoptosis. Surprisingly, several genes involved in the control of the apoptotic pathway were modulated in response to the fusion toxin even though the overall cytotoxic effect on target cells did not include an observable impact on the apoptotic pathway.
A finding of this study is the identification of several genes that are regulated in response to treatment with the VEGF121/rGel fusion construct. Since many of these genes regulate cell adhesion, chemotaxis, and inflammatory responses, the construct may influence tumor development in addition to exerting direct cycotoxic effects on the tumor neovasculature. Therefore, important considerations for future study are the effects of VEGF121/rGel cytotoxicity on tumor endothelial cells and the potential bystander effects of the construct on adjacent tumor cells.
aconfirmed by RT-PCR at 4 and 24 h post-treatment
VEGF121/rGel Inhibits Tube Formation in KDR-Expressing Endothelial Cells
This example investigates the anti-angiogenic effect of VEGF121/rGel in vitro by examining the inhibition of tube formation in receptor-transfected PAE cells.
PAE/KDR and PAE/Flt-1 cells were grown to 80% confluence, detached using Versene, and plated at a concentration of 2×104 cellsper well in a 96-well Matrigel-coated plate under reduced serum (2% FBS) conditions. Cells were treated with 100 nM, 10 nM, 1 nM, 0.1 nM, or 0.01 nM VEGF121/rGel or rGel in triplicate for 24 h. Inhibition of tube formation was assessed by counting the number of tubes formed per well under bright field microscopy. The ability of VEGF121/rGel to inhibit tube formation as a function of incubation time before plating on Matrigel was studied by incubating PAE/KDR cells at the IC50 dose (1 nM) for different periods up to 24 h. Cells were detached and plated in 96-well Matrigel-coated plates under the conditions described above.
As shown in
To determine whether pre-treatment of PAE/KDR cells with VEGF121/rGel affects tube formation, cells were treated with the IC50 dose of VEGF121/rGel for 4, 16, and 24 h, washed with PBS, detached, added to Matrigel-coated plates in VEGF121/rGel-free medium, and incubated for an additional 24 h. Prior incubation of cells with VEGF121/rGel for 16 or 24 h virtually abolished tube formation (
The effect of VEGF121/rGel on tube formation of endothelial cells on Matrigel-coated plates was striking in that cells overexpressing the KDR receptor, but not cells overexpressing the Flt-1 receptor, were affected. This result is consistent with the findings that VEGF121/rGel is cytotoxic only to KDR-expressing endothelial cells and that VEGF121/rGel is internalized only into endothelial cells that express KDR but not Flt-1. The fact that the IC50 dose for cytotoxicity is identical to the IC50 dose for preventing tube formation in PAE/KDR cells suggests that VEGF121/rGel action in vitro immediately disrupts angiogenic tube formation as a temporal prelude to its eventual cytotoxicity to rapidly dividing endothelial cells. Preliminary results examining in vivo endothelialization of Matrigel plugs appear to support the observation that VEGF121/rGel construct can ablate neovascularization at several steps in this complex process.
VEGF121/rGel Inhibits Angiogenesis in the Chorioallantoic Membranes of Chicken Embryos
This example investigates the antiangiogenic effects of VEGF121/rGel in vivo using a chicken chorioallantoic membranes model. Fertilized chicken eggs (SPAFAS; Charles River Laboratories, Wilmington, Mass.) were incubated at 37° C. at 55% humidity for 9 days. An artificial air sac was created over a region containing small blood vessels in the chorioallantoic membranes as previously described (Brooks et al., 1999). A small “window” was cut in the shell after removal of 3 ml of albumen. Filter disks measuring 6 mm in diameter were coated with cortisone acetate in absolute ethanol (3 mg/ml). Each chorioallantoic membranes was locally treated with filter disks saturated with a solution containing bFGF (50 ng/disk) and VEGF121/rGel (1 or 10 nM), rGel (1 or 10 nM), or buffer (PBS). The filter was placed on the chorioallantoic membranes in a region with the lowest density of blood vessels and, as a reference, in the vicinity of a large vessel. Angiogenesis was documented photographically 3 days after treatment. Images were captured using an Olympus stereomicroscope (SZ x12) and Spot Basic software (Diagnostic Instruments, Inc.). The relative vascular density was determined by measuring the area taken up by blood vessels in treated chorioallantoic membranes, normalized to that in chorioallantoic membranes treated with PBS (equal to 100%) (Jiang et al., 2000). This analysis was performed on a Macintosh computer using the public domain NIH Image program. The numbers of blood vessel branch points were quantified by two researchers and compared with the numbers in the treatment controls (Brooks et al., 1999).
As shown in
The following references were cited herein:
Any patents or publications mentioned in this specification are indicative of the levels of those skilled in the art to which the invention pertains. Further, these patents and publications are incorporated by reference herein to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
This continuation-in-part patent application claims benefit of priority of U.S. Ser. No. 10/846,022, filed May 14, 2004, which claims benefit of provisional patent application U.S. Ser. No. 60/476,209, filed Jun. 5, 2003, now abandoned.
This invention was produced in part using funds obtained through Grants 5P30CA16672-26 and P30 CA016672-28 from the National Cancer Institute and Grants ROI CA 7495 and P50 CA91846 from the National Institutes of Health. Consequently, the federal government has certain rights in this invention.
| Number | Date | Country | |
|---|---|---|---|
| 60476209 | Jun 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10919193 | Aug 2004 | US |
| Child | 12552103 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10846022 | May 2004 | US |
| Child | 10919193 | US |
