Patent Application
20160324885
The present invention relates to homo-oligomeric derivatives of a cytidine antimetabolite and its use for the treatment of susceptible disease.
2′.2′-difluoro 2′-deoxycytidine (abbreviated dFdC), also known as gemcitabine, is a synthetic analog of the natural nucleoside deoxycitidine. After uptake through the cell membrane by nucleoside transporters, gemcitabine is converted intracellularly first to difluorodeoxycytidine monophosphate (dFdCMP) by the enzyme deoxycitidine kinase, and subsequently to its active diphosphate (dFdCDP) and triphosphate (dFdCTP) metabolites. During S-phase dFdCTP is incorporated to the nascent DNA chain and this leads to premature chain termination, after addition of one more nucleotide, since the proofreading enzymes are not able to remove dF-cytosine and the DNA polymerases cannot continue the synthesis. Furthermore, the dFdCDP acts as an inhibitor of the enzyme ribonucleotide reductase (RR). RR is the only known enzyme that catalyzes conversion of ribonucleotides to deoxyribonucleotides, and thus it maintains the deoxynucleotide triphosphate (dNTP) pool. Therefore inhibition of RR results in reduction of the dCTP pool, which favors the incorporation of dFdCDP in the newly synthesized DNA. The human RR has three subunits: one large (RRM1) and two small (RRM2 and p53R2) polypeptides. The catalytic form of RR consists of two copies of the large subunit and one copy of each small subunit.
It has been postulated that dFdCDP binds irreversibly to RRM1 and causes its inactivation (Davidson et al., 2004). Further, it has been shown that RRM1 is up-regulated in pancreatic cancer cells resistant to dFdC when compared to the parental cells. In addition, it has been shown a significant correlation between high RRM1 levels and poor survival in pancreatic cancer patients treated with gemcitabine (Nakahira et al, 2007).
Inactivation of dFdC may also be due to the enzyme cytidine deaminase, which converts it to 2,2′-difluorodeoxyuridine (dFdU). In addition, the enzyme 5′-nucleotidase catalyses conversion of nucleotides to nucleosides, thus counteracting the action of nucleoside kinases. Following intravenous administration, dFdC has a short half-life in the human plasma, about 8-17 minutes (Abbruzzese et al, 1991; Reid et al, J 2004), probably because it is rapidly degraded by deaminase in the blood. In tissues, its half-life seems to be longer. It has been shown in mice that radiolabeled dFdC remains up to 3 hours in normal tissues and sarcoma tissue implanted subcutaneously, although the rate of conversion to dFdU was not measured in those studies (Moog et al, 2002; Shipley et al, 1992). It is excreted in the urine mainly as its primary metabolite, dFdU, and only less than 10% is excreted unprocessed (Noble S, Goa K L, 1997; Moog et al, 2002). Thus, only a small amount of dFdC can reach the tumor cells and can be converted into its active dFdCDP and dFdCTP derivatives. This could be one reason why, although gemcitabine exhibits in vitro a strong cytotoxic activity comparable to that of other anticancer drugs such as doxorubicin, for the treatment of cancer patients it has to be administered at the high dose of 1000 mg/m2 of body surface. Such high dose increases the risk of dose-dependent side effects, most notably myelosuppression and hepatic toxicity. Thus, rapid degradation of dFdC in serum, liver and in the tumor tissue by the enzyme cytidine deaminase, which removes the amino group at position 4 of the base, represents an important obstacle for the efficacy of dFdC. In addition, another reason for the need of administrating high doses is that only a fraction of administered dFdC becomes activated by phosphorylation.
Presently, dFdC is the standard chemotherapeutic drug used in the therapy of pancreatic cancer. However, the five-year survival rate of this cancer remains below 5% due to relapse and resistance to dFdC. Therefore, improvements in the chemotherapy based on dFdC are urgently needed.
To date, attempts to overcome the aforementioned problems have failed. Recently, Sampath et al (2010) have described a method based on heteropolymeric compounds comprising long chains of nucleosides or nucleoside analogs, including dFdC, linked by a phosphodiester group. The drawbacks of Sampath's method are twofold. First, the efficacy of heteropolymeric prodrug molecules has not been demonstrated, the main problem being that the active compounds (nucleoside and nucleoside analogs) are linked by nuclease resistant moieties according to the method described by Sampath. Second, no efficient methods are currently available to deliver such long polymeric molecules to cells in vivo. Sampath et al did not report that this method works neither in vitro nor in vivo. In an earlier report, Gmeiner et al described homo-oligonucleotides consisting of monomers of 5-fluoruridine 5′-monophosphate (5-FUMP) or 5-fluodeoxyuridine 5′-monophosphate (5-FdUMP) covalently linked via phosphodiester linkages. The problems of this method are the rapid degradation of the polymers, which may be due to the inherent instability of the compounds used, and the in vivo toxicity.
Furthermore, several strategies have been tried to overcome the rapid degradation of dFdC and improve its stability, bioavailability and anti-tumor activity. Liposomes have been used to protect gemcitabine from degradation. Encapsulation of dFdC into liposomes can be easily achieved, as it is a small molecule, which can diffuse through the liposomal layer (15). Indeed, dFdC has been encapsulated into vesicular phospholipid gel, which showed increased concentration in plasma compared with free dFdC (Moog et al, 2002; Bornmann et al, 2008). However, at physiologic pH dFdC is uncharged and diffuses through the liposomal membrane. In addition, dFdC appears to induce degradation of phospholipids in the liposomal bilayer (Moog et al, 2000). Thus, liposomal dFdC showed increased toxicity, probably due to the uncontrolled release of the drug from the liposomes.
The technical problem underlying the present application could in the broadest sense be seen as dealing with the drawbacks of the prior art. Specifically, the technical problem could be viewed as overcoming low efficacy and resistance of mammalian subjects to dFdC therapy.
The present invention solves the problem of low efficacy of and resistance to dFdC therapy by providing compounds and formulations that increase the efficacy of dFdC in the treatment of patients in need thereof with new compounds and formulations of homo-oligomeric dFdC, which are disclosed in this invention. The present invention relates to the treatment of susceptible infections and dysplastic and neoplastic disorders in an improved manner by administering a dFdC homo-oligomer alone or in combination with protecting carrier and stabilizing and targeting molecules.
Although dFdC has a strong cytotoxic activity in vitro, it has to be administered to cancer patients at high doses (above 1000 mg/m2 per dose), a fact that increases the risk of side effects. In addition, such doses appear to favor the selection of highly resistant clones within the tumor tissue, which are very difficult and often impossible to remove, since the dose of dFdC cannot be increased further.
This invention relates to compounds and compositions that help overcome those problems by combining (i.e. making) molecules of dFdC in oligomeric form. Such oligomeric forms are preferably homo-meric. The term “oligomer” when used herein includes 2-mers, 3-mers, 4-mers, 5-mers, 6-mers, 7-mers, 8-mers, 9-mers, 10-mers, 15-mers, 20-mers, 25-mers or 30-mers of dFdC. A particularly preferred 3-mer is a FpFpFp trinucleotide. Such compositions comprising the compounds of the present invention have, in vitro and in vivo, superior cytotoxic effects at lower doses than dFdC and are effective against tumor cells resistant to this drug. Therefore, they represent a novel anticancer and antiviral agent.
The present invention provides compounds and compositions as well as methods and uses useful for treating cancer, including the following types of neoplasia: neoplasia of the exocrine pancreas, esophagus, stomach, gallbladder, liver, small intestine, vermiform appendix, anus, peritoneum, adenocarcinoma of the colon and rectum; neoplasia of the cervix (cervical intraepithelial neoplasia through invasive cervical cancer), endometrial adenocarcinoma, ovarian cancer, neoplasia of the vulva and vagina, gynecologic sarcomas; neoplasias of the breast; acute and chronic myeloid leukemias, acute and chronic lymphocytic leukemias, hairy cell leukemia, mast cell leukemia, myelodysplastic syndromes, HTLV-1 and T-cell leukemia/lymphoma, Hodgkin's disease, non-Hodgkin lymphomas; renal cell carcinoma, neoplasia of the renal pelvis, ureter, bladder, urethra, prostate, testis, penis; neoplasias of the pituitary, thyroid, adrenal cortex, neuroendocrine and enteropancreatic endocrine system; neuronal neoplasias, medulloblastoma, schwannoma, meningioma, meningeal sarcoma, glioblastoma multiforme, astrocytoma, pineal, oligodendroglial, ependymal and choroid plexus neoplasias; basal cell carcinoma, squamous cell carcinoma, melanoma, dermatofibrosarcoma, Merkel cell tumor, rhabdomyosarcoma, retinoblastoma; head and neck cancer, odontogenic tumors, neoplasias of the oral cavity, pharynx, larynx; large cell lung carcinoma, small cell lung carcinoma, non-small cell lung carcinoma, neoplasias of the thorax, malignant mesothelioma, thymomas; osteogenic sarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, primitive neuroectodermal tumor, angiosarcoma, and Kaposi's sarcoma.
The following disorders are preferred for treatment with the compositions of this invention: pancreatic cancer, hepatocellular cancer, lung cancer, cervical precancer and cancer lesions, breast cancer, ovarian cancer, colorectal cancer and lymphoma, such as non-Hodgkin's lymphoma. The compositions and methods of the present invention are especially useful for the treatment of pancreatic cancer.
The present invention relates to the treatment of susceptible infection or neoplasia with dFdC homo-oligomers.
The present invention also relates to the treatment of susceptible infection or neoplasia comprising separate or simultaneous administration of dFdC homo-oligomers and another anticancer agent.
In a further embodiment, the present invention relates to the treatment of a susceptible infection or neoplasia by administration of dFdC homo-oligomers conjugated to a targeting peptide, aptamer or therapeutic antibody.
In yet another embodiment, the present invention relates to the separate or simultaneous administration of dFdC homo-oligomers conjugated to one or more targeting peptides or therapeutic antibodies and an anticancer agent.
In another aspect, the present invention provides for the use of dFdC homo-oligomers conjugated to targeting peptides or therapeutic antibodies with or without an additional anticancer agent in the manufacture of a medicament for treating susceptible infection and/or neoplasia.
In another embodiment, the present invention relates to pharmaceutical compositions and methods comprising dFdC homo-oligomers, with or without targeting peptides, amino acids or liposomal encapsulation, and therapeutic antibodies for use in therapy, administered simultaneously or sequentially. The dFdC homo-oligomers may also be encapsulated in a liposome.
The compositions of the present invention preferably comprise the compounds as described herein. These compounds are made of 2-30 units of dFdC linked with 5′-3′ phosphate bonds for use in the treatment of susceptible disease. Preferably, these compounds are made of 2-10 units dFdC linked with 5′-3′ phosphate bonds for use in the treatment of susceptible disease. More preferably, the compound is FpFpF.
The main and, thus, preferred purpose of this invention is to provide compositions, compounds and pharmaceutical compositions containing the FpFpF trinucleotide (also referred herein as dFdC trinucleotide) and its derivatives and conjugates as the main active ingredient, as well as specify therapeutically effective dosages resulting as effective as, or more effective than dFdC in the treatment of susceptible disease. The invention described herein is not limited to the specific terminology used, which has been selected for clarity and illustration purposes. Those skilled in the art will appreciate that other compositions and configurations can be conceived preserving the essence and scope of the invention, for example, phosphate derivatives and analogs, as well as nucleotide analogs.
In a first aspect a compound of structural Formula (I) is provided:
or a pharmaceutically acceptable salt, hydrate, N-oxide or solvate thereof, wherein:
R1 is hydrogen, lipid, amino acid, peptide, antibody or aptamer
R2 is hydrogen, lipid, amino acid, peptide, antibody or aptamer
n=1-30
TpF: thymidinyl 3′-5′ phosphate 2′-deoxy-2′,2′-difluorocytidine
FpF: 2′-deoxy-2′,2′-difluorocytidinyl 3′-5′ phosphate 2′-deoxy-2′,2′-difluorocytidine (C18H21O10N6F4P)
FpFpF: 2′-deoxy-2′,2′-difluorocytidinyl 3′-5′phosphate 2′-deoxy-2′,2′-difluorocytidinyl 3′-5′ phosphate-2′-deoxy-2′,2′-difluorocytidine (C27H31O16N9F6P2; pangemine™) 5′-FpFpF-3′-palmitoyl: 2′-deoxy-2′,2′-difluorocytidinyl 3′-5′ phosphate 2′-deoxy-2′,2′-difluorocytidinyl 3′-5′ phosphate-2′-deoxy-2′,2′-difluorocytidinyl 3′-5′ phosphate-1-α(6-(palmitoylamino)hexyl)-2-deoxy-D-ribose
Thus, apart from the preferred FpFpF trinucleotide, the present invention also provides compositions, compounds and pharmaceutical compositions containing dFdC oligomers as described and defined herein and its derivatives and conjugates as the main active ingredient, as well as specify therapeutically effective dosages resulting as effective as, or more effective than dFdC in the treatment of susceptible disease.
The compounds of this invention can be applied therapeutically in an acceptable pharmaceutical composition. They can be used in combination with standard aqueous and non-aqueous vehicles known to those skilled in the art, including sterile water, saline, salts obtained by addition of inorganic or organic acids such as hydrochloric acid and lactic acid, and by addition of inorganic or organic bases like sodium hydroxide and substituted ethanolamine, buffered solutions at physiological pH, Ringer's dextrose, electrolyte replenishers, thickeners, carriers, surfactants, non-aqueous solvents such as polyethylene glycol, ethyl oleate, alcoholic solutions, preservatives and other additives such as chelating agents, antioxidants and antimicrobials.
The dosage should be decided according to the disease to be treated and the clinical history of the patient. Thus, typically the dosage will vary with the age, gender and clinical condition of the patient and should be adjusted by the skilled expert physician. The dosage recommended can be in the range from 0.01 mg/Kg to 100 mg/Kg, preferably in the range 500-1000 mg/m2, in one or more administrations in periods of one or more days, preferably using fixed dose rate by intravenous infusion. However, the dosages used may need to be adjusted according to the toxicological and pharmacokinetic parameters of each particular patient and compound, and to whether the compound is administered alone or in combination with other drugs or if a drug delivery system is used.
The compounds, compositions and methods of the present invention are applied for the treatment or amelioration of the diseases as described herein of mammals, preferably humans.
Apart from the compounds and compositions for use in the methods of treatment as described herein, it is self-explanatory that these compounds and compositions are also applied in methods of treatment of susceptible diseases of mammals, preferably humans, comprising administering a therapeutically effective amount of a composition or compound of the present invention to a mammal, preferably human in need thereof.
Similarly, the present invention relates to the use of the compounds as described herein for the preparation of a medicament (or pharmaceutical composition) for the treatment of susceptible diseases of mammals, preferably humans.
Accordingly, all embodiments described in the context of the compounds and compositions of the present invention are applicable to the methods and uses, mutatis mutandis.
The foregoing is intended to be illustrative and is not intended to limit the invention to the disclosed compounds.
The present invention is described in more detail by the following examples, reference examples and test examples. However, the scope of the present invention is not intended to be limited to these examples.
Methods and results: The synthesis of the various compounds needed for the production of the oligonucleotides tested in this invention was performed as follows:
To a suspension of 2′-deoxy-2′,2′-difluorocytidine (Gemcitabine, F) (1, C16H15F2N2O5, Carbosynth Limited) (1.5 g, 6.35 mmols) coevaporated in anhydrous pyridine and dissolved in dimethylformamide 3.3 ml (15.8 mmols) of hexamethyldisilazane were added. After stirring for 1 hour at room temperature, the solution was concentrated and the residue was dried over toluene. (Rf: 0.6 20% MeOH/DCM). The residue was dissolved in anhydrous pyridine and 1.1 ml of benzoyl chloride (9.52 mmol), were added. After 30 minutes of magnetic stirring the solution was concentrated to dryness and then dissolved in toluene and coevaporated. The residue was dissolved in DCM and washed with 1 M sodium bicarbonate and dried over anhydrous MgSO4 and concentrated to dryness. (Rf. 0.93 7% MeOH). The removal of trimethysilyl protecting group was carried out by the treatment of the residue with a mixture containing 10 ml of dioxane, 10 ml of methanol and 5 ml of NH3 (32%) for 15 min at room temperature. The solution was concentrated, dissolved in dichloromethane (DCM) and washed with a 5% of NaHCO3 and solution saturated of NaCl. Then, the organic phase was concentrated to dryness and the residue was purified by silica gel column chromatography using a gradient of 1% to 4% of methanol (MeOH) in DCM. After concentration of the fractions carrying the desired compound, it was obtained 1.34 g of N4-benzoyl-2′-deoxy-2′,2′-difluorocytidine (2). Yield 62%. C16H15F2N3O5. 1H NMR (300 MHz, CDCl3) δ 3.3 (m, 2H, H-5′), 3.8 (dd, 1H, H-4′), 3.9 (m, 2H, H-5′), 4.3 (m, 1H, H-3′), 6.6 (t, 1H, H-1′), 7.6-7.5 (m, 5H, arom-H), 7.9 (m, 1H, H-5), 8.4 (d, 1H, H-6). MS, expected mass M=367.1. found 368.1 (M+H)+.
To a solution of 2 (1 gr, 2.93 mmols) in anhydrous pyridine 24.4 g (0.2 mmol) of 4-dimethyaminopyridine and 1.09 g (3.2 mmol) of 4,4′-dimethoxytrityl chloride were added. After stirring overnight at room temperature, the reaction was stopped with the addition of 1 ml of MeOH and the resulting solution was concentrated. Then the residue was dissolved in DCM and the organic layer was washed with 5% NaCO3 aqueous solution and saturated NaCl solution and dried over anhydrous MgSO4. Purification was accomplished by silica gel column chromatography eluting with DCM to 2% MeOH/DCM obtaining 0.94 g of 3. Yield 86%. 1H-NMR (300 MHz, CDCl3) δ 3.5 (m, 2H, H-5′), 3.8 (s, 3H, OCH3), 4.1 (dd, 1H, H-4′), 4.5 (m, 1H, H-3′), 6.5 (m, 1H, H-1′), 6.8-7.8 (m, 18H, arom-H), 8.2 (d, 1H, H-5), 8.6 (m, 1H, H-6). MS expected for C37H33F2N3O7: 669.23. Found: 670.23 (M+H)+.
To a solution of 3 (0.5 gr, 0.8 mmols) in anhydrous DCM 0.418 ml (2.4 mmol) of diisopropyethylamine were added together with 0.269 ml (1.2 mmol) of 2-cyanoethyl-N,N-diisopropylchlorophosphoramidite (1.2 mmol, 268 μl) at 0° C. under argon atmosphere. After 15 min the reaction was allowed to reach room temperature and stirred for 1 h. The reaction was quenched with washes of 5% NaHCO3, and saturated NaCl and the organic phase died over anhydrous MgSO4 and concentrated. The residue was purified by silica gel column chromatography (hexanes/EtOAc 1:1+2% Et3N) to give 0.67 g. Yield: 57% of 4 as a mixture of diastereoisomers. 1H NMR (300 MHz, CDCl3) δ 1.0-1.3 (m, 12H, 4 CH3), 2.3 (t, 2H, CH2CN), 2.6 (t, 2H, CH2O), 3.5 (m, 2H, H-5′), 3.6 (m, 1H, CH isp), 3.8 (s, 3H, OCH3), 4.1 (dd, 1H, H-4′), 4.6 (m, 1H, H-3′), 6.5 (m, 1H, H-1′), 6.8-7.8 (m, 18H, arom-H), 8.2 (d, 1H, H-5), 8.63 (m, 1H, H-6), 8.8 (s, 1H, NH). MS expected for C46H50F2N5O8P: 869.34. Found: 870.3 (M+H)+.
First compound 3 is converted to the hemissucinate derivative that is loaded to the amino-control pore glass. Compound 3 (20 mg, 0.031 mmol) was dissolved in DCM and treated with N,N.-dimethylaminopyridine (DMAP, 5.75 mg, 0.047 mmol), and succinic anhydride (4.71 mg, 0.047 mmol). The solution was stirred at room temperature overnight. Then the organic phase was washed with 0.1 M NaH2PO4 and dried over anhydrous MgSO4 and evaporated in vacuo to give compound 5 that was used without any further purification.
2,2′-Dithio-bis-(5-nitropyridine) (0.03 mmols, 9.3 mg) dissolved in acetonitrile/dichloroethane (1:1) was mixed with a solution of succinate derivative 5 (20 mg, 0.031 mmol) and DMAP (0.03 mmol, 3.66 mg) dissolved in 500 μl of acetonitrile. To the clear solution obtained 7.8 mg (0.03 mmol) of triphenylphosphine dissolved in 0.1 ml of acetonitrile were added. The mixture was vortexed and added to a vial containing LCA CPG resin (CPG, Inc.) (200 mg, 71 μmol/g). The solid support was collected by filtration and was washed with CH2Cl2, CH3CN, and subsequently dried under vacuum. The solid support was then suspended in 1 ml of acetic anhydride/pyridine/tetrahydrofuran (1:1:8) and 1 ml of solution (10% N-methylimidazole in tetrahydrofuran) for 30 minutes. The resulting solid support (6) was collected by filtration and washed with MeOH and Et2O, and dried under vacuum. The loading amount was calculated by trityl cation assay with 70% HClO4-EtOH to give 38.4 μmol/g.
Methods and results: Oligonucleotides were synthesized using solid-phase phosphoramidite methodology. Syntheses were run on 1 μmol scale on an Applied Biosystems 3400 synthesizer using 5′-O-DMT-3′-O-(2-cyanoethyl-N,N′-diisopropylphosphoramidite-2′-deoxythymidine and phosphoramidite 4. Controlled-pore glass (CPG) functionalized with 5′-O-DMT-N4-benzoyl-2′-deoxy-2′,2′-difluorocytidine prepared above were used as solid support. The following solutions were used: 0.4 M 1H-tetrazole in ACN (activation); 3% trichloroacetic acid in DCM (detritylation), acetic anhydride/pyridine/tetrahydrofuran (1:1:8) (capping A), 10% N-methylimidazole in tetrahydrofuran (capping B), 0.01 M iodine in tetrahydrofuran/pyridine/water (7:2:1) (phosphate to phosphate oxidation). The coupling time was 15 min for phosphoramidite 4. All oligonucleotides were synthesized in DMT-ON mode. After the solid-phase synthesis, the solid support was transferred to a screw-cap glass vial and incubated at 55° C. for 1 h with 1.5 mL of NH3 solution (33%). The vial was then cooled on ice and the supernatant was transferred into a 2 mL eppendorf tube and evaporated to dryness using an evaporating centrifuge. The residue that was obtained was desalted on a NAP-5 column using water as the eluent and evaporated to dryness. The oligonucleotide was purified by HPLC (DMT-ON). Column: Nucleosil 120-10 C18 (250×4 mm); 20 min linear gradient from 15% to 80% B and 5 min 80% B, flow rate 3 mL/min; solution A was 5% ACN in 0.1 M aqueous triethylammonium acetate (TEAA) and B 70% ACN in 0.1 M aqueous TEAA. The pure fractions were combined and evaporated to dryness. The residue that was obtained was treated with 1 mL of 80% AcOH solution and incubated at room temperature for 30 min. The deprotected oligonucleotide was desalted on a NAP-10 column using water as the eluent. All oligonucleotides were quantified by absorption at 260 nm and confirmed by MALDI mass spectrometry. MALDI-TOF spectra were performed using a Perseptive Voyager DETMRP mass spectrometer, equipped with nitrogen laser at 337 nm using a 3 ns pulse. The matrix used contained 2,4,6-trihydroxyacetophenone (THAP, 10 mg/mL in ACN/water 1:1) and ammonium citrate (50 mg/mL in water) or α-cyano-4-hydroxycinnamic acid (ACH 10 mg/mL in ACN/water 1:1). Dinucleotide TpF: MS expected for C19H23F2N5O11P: 566. Found: 566 (M). Dinucleotide FpF: MS expected for C18H29F4N6O10P: 587. Found: 587 (M). Trinucleotide FpFpF: MS expected for C27H30F6N9O16P2: 913. Found: 913 (M).
The palmitoyl derivative of the trinucleotide was synthesized using solid-phase phosphoramidite methodology as described above. Syntheses were run on 1 μmol scale on an Applied Biosystems 3400 synthesizer using phosphoramidite 4 and the commercially available CPG functionalized with palmitoylamino hexyl 2-deoxyribose (5′-O-(4,4′-dimethoxytrityl)-1-α(6-(palmitoylamino)hexyl)-2-deoxy-D-ribose 3′-O-succinyl-controlled pore glass, Link Technologies) as solid support. After the solid-phase synthesis, the solid support was transferred to a screw-cap glass vial and incubated at room temperature for 4 h with 1.5 mL of NH3 solution (33%)/dioxane (1:1). After filtration of the solid support, the supernatant evaporated to dryness. The residue was purified as described above. Palmitoyl-trinucleotide (5′-FpFpF-3′-palmitoyl): MS expected: 1444. Found: 1444 (M).
Objective: Quantify the cytotoxic activity of dFdC hetero and homo-oligomers in cancer cell lines in comparison with dFdC.
Methods: Cervical cancer cell lines (HeLa, SiHa, CaSki and C-33) were cultured at 37° C./5% CO2 in medium containing DMEM with Glutamax™, 1 mM sodium pyruvate, penicillin/streptomycin (PS) and 10% fetal bovine serum (FBS) (Invitrogen/LifeTechnologies). Pancreatic cancer cell lines were maintained in RPMI 1640 supplemented with Glutamax™, PS and 10% FBS. For the cytotoxicity assay, 96-well plates were plated with 1×104 cells/well. The final volume of culture medium in each well was 100 μL. The cells were treated with different concentrations of drug as indicated. Untreated control cells were set in parallel. The cells were incubated for 72 hours, after which the WST-1 assay (Roche) was performed. This assay utilizes the tetrazolium salt WST-1 [2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium], which is cleaved to a soluble formazan in a process that occurs primarily at the cell surface. Because WST-1 reduction is mostly dependent on the glycolytic production of NAD(P)H in viable cells, the amount of formazan dye formed correlates directly with the number of metabolically active cells in the culture. The cells were incubated with WST-1 for 1 hour at 37° C./5% CO2, then the amount of formazan dye produced was quantified using a scanning spectrophotometer (ELISA plate reader). The absorbance was measured with a test wavelength at 450 nm and a reference wavelength at 630 nm. Then, the 630 nm background absorbance was subtracted from the 450 nm measurement. The mean value of a series of empty wells containing medium but not cells was also subtracted.
Results: 1) The analysis of the cytotoxic effects of a series of different hetero- and homo-oligomers of dFdC that were tested in the HeLa tumor cell line is illustrated in
2) The FpFpF trinucleotide was tested in comparison with dFdC for its ability to inhibit cell growth of tumor cells of different origin: pancreatic cancer (MIA PaCa-2, ASPC) cervical (HeLa, CaSki, C33A) and hepatic (Huh-7) cancers. In all cases the cells were plated the day before treatment to a density of 5000 cells/well in 96-multiwell plates. The cells (6 wells per condition) were treated at the concentrations indicated and incubated for further 72 hours. At this time cell proliferation was quantified using the WST-1 assay as described above. Control wells with untreated cells and without cells were run in parallel. The values obtained with the later were subtracted from all others. Mean values corresponding to wells that were not treated were set to 100% proliferation and the mean values obtained with the treated cells were referred to them. As illustrated in the figures C to I, under these conditions in all cases the FpFpF trinucleotide inhibited cell proliferation with significantly higher efficiency than the dFdC monomer.
Objective: To demonstrate a higher stability of the FpFpF trinucleotide in human serum compared to dFdC.
Methods: The cells were seeded in 96-well plates one day before treatment at a density of 5000 cells/well in 100 μl/well of medium DMEM/Glutamax™/1 mM sodium pyruvate/PS/10%/FBS and cultured at 37° C./5% CO2. Separate serum dilutions of dFdC and FpFpF trinucleotide were prepared from 1 mM stock solutions to a final concentration of 20 μmol/L. The sera aliquots containing either drug were incubated at 37° C./5% CO2 for the indicated times before they were added to the cells to the indicated final concentrations. The cells were incubated for further 72 hours after which the cell proliferation was quantified using the WST-1 assay. Two controls were run in parallel: untreated cells and cells treated with dFdC or FpFpF trinucleotides that were not incubated with serum.
Results: The data obtained with the MIA PaCa-2 and HeLa cell lines are shown in the figures J-K and L-M, respectively. These results obtained with both cell lines show that FpFpF is stable in human serum for at least 2 hours. The inhibition of proliferation with FpFpF in this period remained at about 40%, while the inhibition with dFdC decayed to 5% (HeLa) and 10% (MIA PaCa-2) in the same period of time.
Objective: To demonstrate the anti-proliferative activity of FpFpF trinucleotide in tumor cells with resistance to dFdC
Methods: Wild-type (parental) HeLa cells were sequentially treated with four rounds of increasing concentrations (5 to 40 nM) of dFdC until they became resistant to the drug and were able to proliferate after treatment with dFdC at the highest concentration. The parental and resistant cells were plated one day before treatment at a density of 5000 cells/well in 96-well plates with 100 μl/well of medium DMEM/Glutamax™/1 mM sodium pyruvate/PS/10% FBS and cultured at 37° C./5% CO2. Treatments (6 wells per condition) with wither dFdC or FpFpF were carried out at the concentrations specified in the figures N and O, and the cells were incubated for 72 hours after which proliferation was measured using the WST-1 assay. Untreated cells were used as reference to set the 100% proliferation values.
Results. HeLa cells resistant to dFdC were significantly sensitive to the anti-proliferative effects of FpFpF (compare Figures N and O).
Objective: To prove and quantify the inhibition of cell proliferation caused by FpFpF trinucleotide conjugated to a peptide that specifically binds tumor cells
Methods: Targeted therapies are intended to enhance accumulation of chemotherapy drugs into tumor cells thereby causing a more potent cytotoxic effect. One way to achieve this is using peptides binding surface proteins on tumor cells with high affinity. One such peptide, H2N-SPRGDLAVLGHKY-COOH (HBP-1) (SEQ ID No: 1) (Nothelfer et al, 2009), has been previously shown to bind tumor cells via the intrinsic RGD motif. This peptide was synthesized, purified and conjugated to FpFpF or dFdC using the water-soluble carbodiimide cross-linker EDC (Thermo Scientific Pierce) following the manufacturer instructions. Excess reagent and cross-linking byproducts were removed by successive passes through two Sephadex G-25 columns. The concentration of peptide in the cross-linked product was determined by the BCA method (Thermo Scientific Pierce) and the concentration of dFdC or FpFpF bound to peptide in the purified conjugates (abbreviated P-dFdC and P-FpFpF, respectively) was measured spectrophotometrically (A260 nm) against standard curves.
Results. The effects of P-dFdC and P-FpFpF on proliferation of the pancreatic cancer cell lines BxPC-3 and MIA PaCa-2 are shown in the
Objective: Improve the cell permeability and activity of FpFpF in tumor cells
Methods: The FpFpF trinucleotide was coupled to lipid as described in the Example 3 for the Palmitoyl-trinucleotide (5′-FpFpF-3′-Pal). Panc-1 cells were plated one day before treatment at a density of 5000 cells/well in a 96-well plate with 100 μl/well of medium RPMI/Glutamax™/1 mM sodium pyruvate/PS/10% FBS and cultured at 37° C./5% CO2. Treatments (6 wells per condition) with wither dFdC, FpFpF and FpFpF-Pal were carried out at the indicated concentrations.
Results: The FpFpF-Pal derivative exhibited the highest inhibitory power with an ID50 of 0.28 μM compared to 12.17 and 5.52 μM for dFdC and FpFpF, respectively.
Objective: To improve FpFpF trinucleotide delivery through liposome encapsulation
Methods. Naked or antibody-targeted liposomes (LPs) carrying anticancer compounds may increase the therapeutic efficacy of these agents. The lipids were hydrated in saline solution for two hours at room temperature (LPs). Then, the reconstituted LPs were diluted with 1 ml of saline solution and applied to Amicon Ultra-4 NMWL100 kDa centrifugal filters (Millipore) and washed three times with 1 ml of saline solution. Maleimido-activated phospholipids are suitable for reaction with sulfhydryl groups on antibodies. For conjugation of anti-Muc1 antibodies to liposomes, antibody was added to a final concentration of 40 μg/ml (Ab-LPs). The mixture was incubated at ambient temperature for two hours. MCF-7 cells (106 cells/ml) were incubated in medium RPMI with either 1) gemcitabine, 2) dFdC homo-oligomers, or 3) 1 mg(LP)/ml Ab-LPs. After 30 minutes equal aliquots of the cells were centrifuged and washed twice with RPMI medium.
Results: Compared with unencapsulated FpFpF, the FpFpF trinucleotide showed higher inhibitory activity on proliferation of the Panc-1 and BxPc-3 cell lines.
Objective: To compare the anti-tumor activities of FpFpF trinucleotide and dFdC in vivo in a xenograft model. HeLa cells and immunodeficient mice were used in this assay as described below.
Methods. Immunodeficient CAnN.Cg-Fox1nu/Cr1 (BALB/c) mice (The Jackson Laboratories) are well suited for the xenotransplantation of human tumors. HeLa cells (5×106) were mixed 1:1 with matrigel in a final volume of 0.1 ml and then injected subcutaneously in the right flank of each mouse. Treatments were initiated at the time when the tumor volume reached approximately 200 mm3. The drugs (FpFpF trinucleotide or dFdC) were administered intraperitoneally at 10 mg/kg every fourth day for a total of four doses. Tumor volumes were calculated with the ellipsoid volume formula (L×W×H×π/6) (Tomayko and Reynolds, 1989). Tumor volume values were transformed to a log scale. A two-way analysis of variance by time and treatment was used. The data are finally expressed as means and standard errors for each treatment group against time. A Weibull distribution was assumed to calculate mean times and standard errors for each treatment group. Tumor growth delay was defined as the difference in mean time between each treated group and the control group.
Results. Data in Table 1 show the effects of FpFpF trinucleotide in comparison with dFdC. Treatment with FpFpF trinucleotide caused a statistically significant delay (p<0.01) in tumor growth compared to dFdC.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/064604 | 7/10/2013 | WO | 00 |
