Patent Application
20070178045
The objects of the present invention are compounds useful as medicaments, processes for the preparation thereof, pharmaceutical compositions containing them and uses thereof for the preparation of medicaments useful for the therapy of diseases due to abnormal angiogenesis.
In oncological patients, chemotherapy is, in many cases, the only treatment option for disseminated cancer. One approach to improve the efficacy and reduce the toxicity of anticancer chemotherapy is to administer drugs that target the receptors involved in tumour angiogenesis.
Integrins are involved in the adhesion between one cell and the other and between cells and the extracellular matrix both in the process of tumour angiogenesis and in the metastatic process. In particular, αvβ3 and αvβ5 integrin receptors are strongly expressed in the endothelial cells of human tumour microvessels and in the tumour cells themselves.
The tumour vascularisation is now generally recognised as being a promising target for anticancer therapy [H. Jin and J. Varner, Br. J. Cancer, 2004, 90(3): 561-5].
In recent years, numerous studies have demonstrated that cyclopeptide derivatives containing the Arg-Gly-Asp sequence present high affinity for integrin receptors.
Inhibition of tumor progression and neoangiogenesis using cyclic RGD-peptides is being investigated and some studies have already shown promising results.
For example it has recently been demonstrated in a chemically induced colon carcinoma in rats that late onset of treatment with integrin-blocking peptides resulted in an inhibition of tumour growth and a reduced tumour load which appeared to be mediated, at least in part, by inhibition of neoangiogenesis (Haier J. et al, Clin Exp Metastasis. 2002; 19(8):665-72). Therefore αvβ3-integrin-receptor inhibition appears to be a good therapeutic strategy for cancer.
Moreover these cyclic RGD peptides may also have interesting therapeutical applications in cardiovascular diseases, osteoporosis and viral infections utilising cellular integrins for their penetration into the target cells (e.g. HIV). Such compounds are useful for directing chemotherapy drugs, particularly anticancer drugs, against those cells that express high levels of integrin receptors. In this way, an efficacious therapeutic response is achieved with reduced side effects induced by the chemotherapy agent.
The present invention relates to cyclopeptide derivatives endowed with anti-integrin activity, and particularly to cyclic peptides containing, in addition to a sequence of three amino acids which is constant in all the compounds described herein, other two residues consisting in natural and non-natural amino acids, that can be substituted on the nitrogen or on the Cα with a residue consisting in a functional group, or in a terminal chain with a functional group that unexpectedly enhances its binding to integrins αvβ3 and αvβ5. The present invention also relates to processes for the preparation of said compounds, the use thereof as medicaments, particularly as integrin receptor inhibitors, with an action useful in the treatment of diseases such as retinopathy, acute renal failure, osteoporosis and metastases and to pharmaceutical compositions containing them. These compounds, when suitably labelled, are also useful as diagnostic agents for the detection of small tumour masses and arterial occlusion events.
The drugs vehicled by the cyclopeptides according to the present invention belong to cytotoxic agent classes such as alkylating agents (cyclophosphamides, nitrosoureas), antimetabolites (methotrexate, 5-fluorouracyl, cytosine arabinoside), natural products (doxorubicin and structural analogues, actinomycin D, bleomycin, vinca alkaloids, epipodophyllotoxins, and mitomycin C).
For an exhaustive description of the state of the art regarding the αvβ3 and αvβ5 integrin receptor compounds and their applications, the reader is referred to WO 2004/011487, in the name of the Applicant, to which explicit reference is made also in connection with the scientific background.
Surprisingly, the resultant molecules of the present invention demonstrate affinity for integrins, which is sometimes considerably greater than that observed for the cyclopeptides belonging to the same class and described in the literature [H. Kessler, et al., J. Med. Chem., 1999, 42, 3033-40].
Therefore, this invention provides integrin inhibitors of the αvβ3 and αvβ5 type, which are much more potent than the known compounds.
Therefore, the main object of the present invention are compounds of Formula I, as follows:
c(R1-Arg-Gly-Asp-R2) (Formula I)
where:
Preferred examples of formula (I) compounds are:
What is meant by pharmaceutically acceptable salt is any salt that does not give rise to toxic or side effects.
Such salts are well known to pharmacologists and to experts in pharmaceutical technology.
The compounds of Formula I may be prepared according to the process described here below and exemplified for the preferred compounds according to the invention. This process constitutes a further object of the invention.
The compounds of Formula I can be prepared, after synthesising the non-natural amino acid residues, according to the conventional techniques of peptide synthesis, as described in the examples in the experimental part. The peptide synthesis can be accomplished either in the solid phase or in solution. Once the suitably protected linear peptide has been prepared, it is cyclised.
The compounds described in the present invention are integrin inhibitors and therefore are useful as medicaments in the treatment of cancer, as diagnostic imaging agents and as targeted drug vectors (G. C. Tucker 2003 Curr. Opin. Investig. Drugs 4, 722-31), particularly for the treatment of tumours whose cells overexpress integrins both naturally and in an induced manner, for example, as a result of radiotherapy; in inflammatory diseases, (e.g. rheumatoid arthritis), in the diseases underlying abnormal angiogenesis, such as tumours, retinopathy, eye diseases, acute renal failure, osteoporosis and metastasis, cardiovascular diseases (stroke and heart damage), and restenosis after percutaneous transluminal coronary angioplasty (J. S. Kerr et al. Drug News Perspect 2001, 14, 143 50). The compounds described herein are also useful, when suitably labelled, as diagnostic agents, especially for the detection of small tumour masses and arterial occlusion events. Various antagonists have been labelled with (18)F, (111)In, (99)Tc, (90)Y and many iodine isotopes, to monitor tumour-induced angiogenesis, since integrins are involved in the migration of endothelial cells for the formation of new vessels (R. H. Haubner et al. 2003 Q. J. Nucl. Med. 47 189-99). High-affinity radiolabelled peptides can be used as targets for αvβ3 integrins and in order to image the areas of vascular damage, inasmuch as αvβ3 integrin expression is increased in the activated endothelial cells and in the vascular smooth muscle cells after vascular damage. This approach overcomes the shortcomings of the magnetic resonance and computed axial tomography imaging methods such as the lack of biologically relevant ligands and blood contrast agents for imaging (F. G. Blankenberg et al. 2002 Am. J. Cardiov. Drugs 2, 357-65).
The pharmaceutical compositions contain at least one compound of Formula I as the active ingredient in an amount such as to produce a significant therapeutic effect. The compositions according to the present invention are entirely conventional and are obtained using methods which are common practice in the pharmaceutical industry. According to the administration route selected, the compositions will be in solid or liquid form, suitable for oral, parenteral or intravenous administration. The compositions according to the present invention contain, along with the active ingredient, at least one pharmaceutically acceptable vehicle or excipient. Particularly useful may be formulation adjuvants, such as, for example, solubilising agents, dispersing agents, suspension agents and emulsifying agents.
The compounds of Formula I can also be used in combination with other anticancer drugs or with other drugs with antiparasite or antiviral activity, both in separate forms or in single dosage form.
The medicaments which are the object of the present invention are also used in the treatment of parasite and adenovirus diseases. Entry of the pathogens into the cells occurs by means of direct penetration of the plasma membrane, clathrin-mediated endocytosis, caveolar endocytosis, pinocytosis or macropinocytosis. Macropinocytosis requires the involvement of integrins (O. Meier et al., 2003, J. Gene Med. 5, 451-62). The antiparasite activity can be exerted then by inhibition of integrin-mediated adhesion and by recruitment of leukocytes guided by the chemokine receptors, e.g. in the control of inflammation induced by Trypanosoma cruzi. Incidentally, in the acute phase of Chagas disease, induction of the inflammatory process is crucial for the control of Trypanosoma cruzi in the target tissue of the host/parasite equilibrium (J. Lannes-Vieira, 2003, Mem. Inst. Oswaldo Cruz, 98, 299-304).
The following examples further illustrate the invention.
The abbreviations used are:
1.587 mmol of Fmoc-Gly-Res (Res=Sasrin Resin®, Bachem) were suspended under stirring in 75 ml of DMF for 30 minutes, after which 18 ml of piperidine were added, continuing the stirring for a further 30 minutes. The resin, filtered and washed with DMF, was suspended in 50 ml of NMP (N-methyl-pyrrolidone) for 15 minutes, after which Fmoc-Arg(Pmc)-OH, HOBT, TBTU and DIEA were added (3.174 mmol of each); after 2 hours of stirring, the suspension was filtered and washed with DMF. After deprotection with piperidine, the condensation was repeated with the other amino acids in succession, operating each time as described above, namely: Fmoc-Amp(Cbz)-OH, Fmoc-D-Phe-OH, and Fmoc-Asp(OtBu)-OH. After the last deprotection of the Fmoc-N-terminal, the linear pentapeptide is released from the resin with 45 ml of 1% TFA in DCM. This is dissolved in approximately 1 l of CH3CN, and 4.761 mmol of HOBT and TBTU, and 10 ml of DIEA are added; the solution is left to stir for 30 minutes, the solvent is evaporated to a small volume and the precipitation of the product is completed with water.
The filtered crude product was dissolved in thioanisol (50 eq) and TFA (270 eq) and left to stir overnight at room temperature.
The reaction mixture was brought to dryness and the residue taken up with the minimum amount of TFA and re-precipitated with excess ethyl ether. Finally, the crude product was purified by RP-HPLC [Column: Alltima C-18, Alltech; mobile phase: 17% CH3CN in water+0.1% TFA].
Analytical HPLC: column: Purosphere STAR, Merck; mobile phase: 15% CH3CN in water+0.1% TFA): Rt=12.15 min.
Molecular mass=652
0.69 mmol of Fmoc-Gly-Res were treated exactly as described in example 1, with the difference that in this case the third and fourth amino acids were added in the form of dipeptide Fmoc-D-Phe-Aad(OBzl)-OH. After deprotection of the benzylester by means of CTH, and purification of the crude product with preparatory RP-HPLC (mobile phase: CH3CN 55% in water+TFA 0.1%; Rt=17.29 minutes), 187 mg of pure deprotected peptide were obtained. This was dissolved in TFA and, after 1 hour at room temperature, the solution was brought to dryness. The residue was re-dissolved in the minimum amount of TFA and precipitated with excess ethyl ether. The operation was repeated until the clean final product was obtained.
Analytical RP-HPLC (17% CH3CN in water+0.1% TFA), Rt=12.52 mm.
Molecular mass=619
To a suspension of Fmoc-Phe(4-Pht-N—CH2)—COOH in anhydrous toluene brought to reflux 2 eq of CSA and 20 eq of paraformaldehyde divided into 4 portions at intervals of 15 minutes were added. The mixture was allowed to cool, diluted with 120 ml of toluene and washed with 5% NaHCO3 and water. After evaporation of the solvent, the residue was dissolved in 15 ml of CHCl3+15 ml of TFA+700 μl of Et3SiH; the mixture was left in the dark to stir for 42 hours. After evaporation of the solvent, the residue was purified by filtration on silica gel. Overall yield: 90%.
The linear peptide was synthesized in solid phase as described in Example 1, inserting Fmoc-N-Me-Phe-(4-Pht-N—CH2)—COOH as the third amino acid, prepared as described above. In this case the deprotections of N-Fmoc-terminal on resin were carried out with 30% diisopropylamine (300 eq) in DMF solution (due to the presence of phthalimide). After cyclisation, 500 mg of the peptide were dissolved by heating in 10 ml of absolute EtOH, to which 0.9 ml of a solution of NH2—NH2.H2O 1M in ethanol were added. After heating at reflux for 2 hours, the solvent was evaporated and the residue taken up with 10 ml of DCM+10 ml of Na2CO3 solution with vigorous shaking. After evaporation of the organic phase, the crude residue was purified by preparatory RP-HPLC (mobile phase: 17% CH3CN in water+0.1% TFA).
Analytical RP-HPLC (16% CH3CN in water+0.1% TFA), Rt=11.7 min
Molecular mass=665
120 mg of cyclopeptide c[Arg(Pmc)-Gly-Asp(OtBu)-D-Phe-Amp].TFA (prepared as described in example 1) were dissolved in 3.6 ml of a mixture of DCM-DMF 2:1, together with a stoichiometric amount of TEA and succinic anhydride. After 1 hour the reaction mixture was diluted with 30 ml of DCM and washed with water. The organic phase, dried and concentrated, yielded a residue of 100 mg of hemisuccinate. This product was completely deprotected with TFA and then submitted to a first purification, as already described in the examples above. It was then further purified by preparatory RP-HPLC (23% CH3CN in water+0.1% TFA).
Analytical RP-HPLC: (20% CH3CN in water+0.1% TFA), Rt=14.66 mm.
Molecular mass=751
To a solution of 1.22 mmol of Boc-monoprotected p-xylylenediamine in 6 ml of THF were added 1.83 mmol of TEA and, dropwise, a solution of 1.22 mmol of benzyl bromoacetate in 2 ml of THF. The mixture was left to stir overnight, after which the solvent was evaporated and the residue purified on a flash chromatography column (CHCl3-EtOAc, 9:1). 0.69 mmol of N-(4-Boc-NH—CH2-benzyl)-glycine benzylester were obtained.
250 mg of Fmoc-D-Phe-OH were dissolved in 27 ml of DCM and 40 μl of diphosgene and 230 μl of sym-collidine were added; after 15 minutes 190 mg of the previously prepared ester were added, dissolved in 3 ml of DCM. After 3 hours, 80 μl of N-Me-piperazine were added to the reaction mixture and stirred for 10 minutes, after which the mixture was diluted with 10 ml of DCM and extraction was done with water, HCl 0.5 N, water, 5% NaHCO3 and water. After evaporation of the solvent, the residue was purified by flash chromatography on silica gel (DCM-EtOAc, 9:1). Yield: 80%.
To 100 mg of the product thus obtained, dissolved in 6 ml of MeOH, were added 76 μl of AcOH and 42 mg of HCOONH4, and the mixture cooled to 0° C., and 50 mg of 10% Pd/C were added. After 30 minutes, the reaction mixture was filtered on celite. The filtrate was brought to dryness and purified on a flash chromatography column (CHCl3—MeOH 9:1). Yield: 90%.
190 mg of the product thus obtained were dissolved in 1.2 ml of TFA and brought to dryness (deprotection of Boc); the residue was redissolved in 9 ml of 10% Na2CO3+6 ml of dioxane, cooled to 0° C. and a solution of 120 μl of benzyloxycarbonyl chloride diluted with 3 ml of dioxane was added dropwise. After 1 hour of stirring at room temperature. evaporation was carried out under vacuum to a small volume, after which the mixture was diluted with water, the pH was reduced to 1 with HCl and extraction was done with EtOAc. After evaporation of the solvent, the residue was purified by filtration on silica gel, washing with CHCl3—MeOH 8:2). Pure dipeptide yield: 82%.
0.69 mmol of Fmoc-Gly-Res were treated as described in example 1. After Arg, the previously prepared dipeptide Fmoc-D-Phe-N(4-Cbz-NH—CH2-benzyl)-Gly was added in sequence. The crude product was dissolved in thioanisol and TFA and left to stir at room temperature for 4.5 hours. The first purification was done as described in the other examples, while the final purification was done with preparatory HPLC (mobile phase: 16% CH3CN in water+0.1% TFA).
Analytical RP-HPLC (15% CH3CN in water+0.1% TFA), Rt=7.67 mm.
Molecular mass=652
To a solution of 200 mg of c(Arg(Pmc)-Gly-Asp(OtBu)-D-Phe-Amp).TFA (obtained as described in example 1) in 4 ml of a 3:1 DCM-DMF mixture was added a substantial excess of glycol diacid. DIEA (3 eq) and DCC (2 eq) were added to the same solution. The mixture was left to stir overnight, after which it was diluted with DCM and washed with water.
The crude product was recovered by evaporating the organic phase and purified by flash chromatography (mobile phase: CHCl3—MeOH 7:3+1% AcOH); the fractions containing the product were pooled, washed with water, dehydrated and brought to dryness, and yielded a residue of 157 mg of pure product. This was treated with TFA for 1.5 hours and cleaned as described in the other examples, after which the final purification was done by preparatory HPLC (mobile phase: 22% CH3CN in water+0.1% TFA).
Analytical RP-HPLC: (23% CH3CN in water+0.1% TFA); Rt=10 min.
Molecular mass=855
150 mg of the peptide described in example 1 and 110 mg of PEG 600-COOFm (1 eq)+HOAT (1.5 eq)+DIEA (2 eq) were dissolved in 6 ml of a mixture of DCM-DMF (2:1), and the solution cooled to 0° C.; 1.5 eq of DCC were added and the mixture was left to stir overnight. After evaporation of the solvent, the residue was purified on a flash chromatography column (step I: CHCl3—MeOH, 96:4; step II: CHCl3—MeOH, 90:10. For the deprotection of the fluorenylmethylester, 36 mg of the ester were dissolved in 1.8 ml CHCl3, 41 μl (20 eq) of piperidine were added and left for 1 night at room temperature. After evaporation of the solvent, the crude residue was purified by preparatory HPLC (46% CH3CN in water+0.1% TFA). The pure product thus obtained was dissolved in TFA and left for 2 hours at room temperature. After reduction to a small volume, the totally deprotected product was precipitated with excess ethyl ether.
Analytical RP-HPLC (26% CH3CN in water+0.1% TFA); Rt=7.89-15.83 min.
Molecular mass: 1119.
Arg(Pmc)-Gly sequence was obtained by solid-phase synthesis in according to the process above described, while the building block oNbs-N[CH2)5—COOAll]Val-OH was introduced by the following process:
The mixture of building block (3 eq) (synthesis described below) and 1-bromo-N,N-2-trimethyl-1-propenylamine (4.5 eq) was dissolved in DCM under inert atmosphere (Argon), continuing the stirring for 10 minutes at room temperature.
Then the mixture was added to the resin in DCM with collidine (12 eq), under inert atmosphere. After 2 hours (Kaiser test negative), the resin was filtered and abundantly washed with DCM e DMF, and dried under reduced pressure.
To carry out the 2-nitrobenzene sulfonyl (oNbs) moiety deprotection, 2-mercaptoetanol (10 eq)+DBU (5 eq) in DMF, were added to the resin. After 30 minutes the same reagents were added again and, after 2 hours, the cleaving was complete (checked via HPLC). The resin was filtered and washed with DCM and DMF.
The synthetic route of the next coupling was the same, using N3-D-Phe-Br. The corresponding α-azide acid was prepared by “diazotransfer” reaction starting from the corresponding aminoacid [Alper et al, Tetrahedron Lett. (1996) 37, 6029]. The azide moiety was reduced using a solution of SnCl4 (10 eq)+thiophenol (40 eq) and TEA (10 eq) in DMF. Such solution was added to the resin in DMF and left under stirring for 1 hour. Then the resulting suspension was treated with 2N NaOH for 5 minutes, filtered and washed with water, DMF, MeOH, DMF e DCM.
Subsequently the conditions for the Asp condensation, the following deprotection of the Fmoc group, the cleavage of the resin and the cyclization of peptide were those commonly used in the peptide chemistry synthesis.
The raw material was purified by flash chromatography.
The peptide obtained was deprotected step by step, first using Pd (Ph3P)4 and then with TFA.
The final product was purified by precipitation with TFA/diethylether.
To a solution of hydroxyacid HO—(CH2)5COOH and absolute ethanol, Cs2CO3 (1 eq) was added. The mixture was left to stir until the total dissolution of the salt (about 40 minutes). The solvent was evaporated under vacuum and the residue dried with benzene until to obtain a white solid crystal. To that solid, dissolved in DMF, allyl bromide (11 eq) was added and left under stirring for 2 hours. Further allyl bromide was added (11 eq) and left to stir at room temperature overnight. The raw material was purified by flash chromatography (exane/AcOEt, 1:1). Yield 70%.
To a solution of oNbs-Val-OtBu in THF, at 10° C., have been added hydroxyester (1.05 eq) and triphenylphosphine (1.5 eq) . At −20° C. 4.08 ml of DEAD (40% in toluene) was added. After stirring at room temperature for 48 hours, the solvent was evaporated and the raw material was purified by preparatory RP-HPLC. (CH3CN/H2O/TFA: 75-25-0.1). Yield 70%.
After the final deprotection of tert-butilic ester with TFA, the desiderated building block was obtained.
This peptide was synthesized by solid phase as described in the Example 1, inserting Fmoc-Amp(CO—CH2-Teg)-OH as the third amino acid, which was prepared as following:
570 mg of CH3O(CH2CH2O)3—CH2—COOH, 473 mg of 2,3,4,5-pentafluorophenol (Pfp) and 207 μl of pyridine were dissolved with 11.4 ml of DCM. To the solution, cooled to 00 C, 637 mg of DCC were added and the reaction mixture left under stirring for 1.5 h. After filtration and washing the filtrate with water, 1 N HCl, water, 5% NaHCO3 and water, the organic solution was taken to dryness, giving 984 mg of the raw ester.
To a suspension of 500 mg of Fmoc-aminomethylphenylalanine. TFA salt in 15 ml of DCM, 260 μl of TEA was added followed by 800 mg of the activated ester and the mixture left under stirring for 3 h. The crude product was purified by flash chromatography, affording the pure building block.
The final cyclic peptide was puified as usual and isolated from preparative HPLC (27% CH3CN in water+1% TFA), Rt=12.7 min.
Molecular mass=855
Binding to Integrin αvβ3 Receptors
The purified αvβ3 receptor (Chemicon, cat. CC1020) was diluted in buffer (20 mM Tris, pH 7.4, 150 mM NaCl, 2 mM CaCl2, 1 mM MgCl2, 1 mM MnCl2) to a concentration of 0.5 μg/ml. An aliquot of 100 μl was added to 96-well plates and incubated overnight at +4° C. Plates were washed once with buffer (50 mM Tris, pH 7.4, 100 mM NaCl, 2 mM CaCl2, 1 mM MgCl2, 1 mM MnCl2, 1% bovine serum albumin) and then incubated for another 2 hours at room temperature. Plates were washed twice with the same buffer and incubated for 3 hours at room temperature with the radioactive ligand [125I]echistatin (Amersham Pharmacia Biotech) 0.05 nM in the presence of competition ligands. At the end of incubation, the wells were washed and the radioactivity determined using a gamma counter (Packard). Non-specific binding of the ligand was determined in the presence of excess cold echistatin (1 μM).
Binding to Integrin αvβ5 Receptors
The purified αvβ5 receptor (Chemicon, cat. CC1020) was diluted in buffer (20 mM Tris, pH 7.4, 150 mM NaCl, 2 mM CaCl2, 1 mM MgCl2, 1 mM MnCl2) to a concentration of 1 μg/ml. An aliquot of 100 μl was added to 96-well plates and incubated overnight at +4° C. Plates were washed once with buffer (50 mM Tris, pH 7.4, 100 mM NaCl, 2 mM CaCl2, 1 mM MgCl2, 1 mM MnCl2, 1% bovine serum albumin) and then incubated for another 2 hours at room temperature. Plates were washed twice with the same buffer and incubated for 3 hours at room temperature with the radioactive ligand [125I]echistatin (Amersham Pharmacia Biotech) 0.15 nM in the presence of competition ligands. At the end of incubation, the wells were washed and the radioactivity determined using a gamma counter (Packard). Non-specific ligand binding was determined in the presence of excess cold echistatin (1 μM).
Evaluation of IC50 Parameters
The affinity of the products for vitronectin receptors was expressed as IC50 value±SD, i.e. as the concentration capable of inhibiting 50% of the specific radioligand-receptor binding. The IC50 parameter was elaborated using “ALLFIT” software.
Results
All the RGD peptides examined showed significant affinity for αvβ3 and αvβ5 integrin receptors with an IC50 value of the order of nanomoles. In particular, the most active in inhibiting echistatin binding to the αvβ3 integrins was ST2581 (IC50=1.7 nM) followed by the products ST2661 and ST2700 (IC50=4 and 7 nM), while the most active for the αvβ5 integrin receptors was the product ST2650 (IC50=0.17 nM) followed by the molecules ST2661 and ST2700 (IC50=0.35 and 0.99 nM, respectively).
Although the main function of integrins is to mediate cellular adhesion to ECM proteins in intercellular spaces and basement membranes, they also transduce intracellular signals that promote cell migration as well as survival. Integrins have no intrinsic enzymatic activity but activate signaling pathways by coclustering with kinases and adaptor proteins in focal adhesion complexes after their association with polyvalent extracellular matrix (ECM) proteins. For example, integrin ligation suppresses apoptosis by activating suppressors of apoptosis and by inhibitin caspase activation. Integrin also stimulate cell migration by activating Rho and Rac GTPases (guanosine triphosphatases) and by anchoring actin filaments to the membrane. These adhesion proteins promote cell cycle entry by stimulating expression of cyclins. Integrin ligation, therefore, supports signal transduction cascades that promote cell proliferation, survival and migration. In contrast, inhibition of cell integrin-ligand interaction, inhibits cell migration and proliferation and induces apoptosis (Jin H. and Varner J. 2004 Br. J. Cancer 90, 561-565).
Adhesion Assay of Tumor Cells on Vitronectin
A2780 human ovarian carcinoma and PC3 prostate carcinoma cells were grown in RPMI 1640 containing 10% fetal bovine serum and 50 μg/ml gentamycin sulfate. A498 human renal carcinoma were grown in EMEM containing 10% fetal bovine serum and 50 μg/ml gentamycin sulfate. All the cells were maintained in a 37° C. incubator with saturated humidity and an atmosphere of 95% air and 5% CO2.
A2780 cell line expresses high levels of αvβ5 integrins, A498 high levels of αvβ3 integrins, and PC3 low levels of both integrins.
To test the effect of the drugs on cell adhesion, the appropriate cellular density (40000-50000 cells/well) for each tumor cell line was incubated with different concentrations of the compounds in 96-well tissue culture plates coated with vitronectin (5 μg/ml) and was allowed to attach for 3 hours. After this time the cells were washed once with PBS containing Ca2+ e Mg2+. Tumor cells were fixed with 4% paraformaldehyde for 10 min at room temperature and stained with 1% toluidine blue for 10 min at room temperature. Tumor cells were washed with bi-distilled water, dried and solubilized with 1% SDS. The number of adherent cells was determined in a microplate reader (Victor2, EG&G Wallac) at 600 nm.
An IC50 value as parameter to measure the inhibiting effect of the molecules on tumor cell adhesion to vitronectin was evaluated using “ALLFIT” computer program. The results obtained with the tested compounds according to the invention are reported in Table 2.
| Number | Date | Country | Kind |
|---|---|---|---|
| RM2004A000239 | May 2004 | IT | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IT05/00262 | 5/4/2005 | WO | 11/13/2006 |
