Antiproliferative effects of PCA‐4230, a new antithrombotic drug, in vascular smooth muscle cells

In the present study we examined the effects of PCA‐4230, a novel antithrombotic agent, on the growth of cultured A10 vascular smooth muscle cells (rat aorta). The action of PCA‐4230 on cell proliferation and on serum‐induced DNA synthesis was determined by measuring the cell number and the incorporation of the thymidine analogue 5‐bromo‐2′‐deoxyuridine (BrdU), respectively. PCA‐4230 reversibly inhibited vascular smooth muscle cell proliferation. The increase in cell number was significantly reduced in the presence of 1 and 50 μ m PCA‐4230. DNA synthesis was concentration‐dependently inhibited by PCA‐4230 (0.5 to 50 μ m ) in A10 cells that were synchronized by 48 h serum starvation and then re‐stimulated by serum repletion, with an IC 50 value of 13 μ m . However, serum‐induced DNA synthesis in bovine aortic endothelial cells was not significantly affected by PCA‐4230. In addition, PCA‐4230 (50 μ m ) caused a significant drop in PDGF‐BB‐mediated BrdU incorporation in A10 cells. The effect of PCA‐4230 on serum‐induced DNA synthesis was compared to that elicited by nifedipine, another dihydropyridine‐class inhibitor of vascular smooth muscle proliferation. PCA‐4230 (10 μ m ) elicited a degree of inhibition similar to that of nifedipine at equimolar concentration. To define the nature of the cell proliferation inhibition, an evaluation of cell cycle progression was undertaken. Flow cytometry studies of DNA content in synchronized cells revealed a block of the serum‐inducible cell cycle progression. This inhibitory effect was markedly reduced when PCA‐4230 was added 2 h after serum repletion. Accordingly, PCA‐4230 (50 μ m ) caused a 95 and 90% decrease in the elevation of c‐ fos and c‐ jun proto‐oncogenes expression as evaluated by Northern blot analysis of mRNA induced early after serum addition. The present results indicate that PCA‐4230 inhibits vascular smooth muscle cell proliferation, in culture, by altering the cell cycle progression. Flow cytometric studies of DNA content and the down regulation of c‐ fos and c‐ jun proto‐oncogenes, suggest that the drug is acting at the early G 0 /G 1 transition phase. PCA‐4230 may hold promising potential for the prevention of structural abnormalities of blood vessels associated with atherosclerosis and vascular diseases.British Journal of Pharmacology (1997) 120 , 1360–1366; doi: 10.1038/sj.bjp.0701035