Fukuoka K, Usuda J, Iwamoto Y, Fukumoto H, Nakamura T, Yoneda T, Narita N, Saijo N, Nishio K
Pharmacology Division, National Cancer Center Research Institute, Tokyo, Japan.
Invest New Drugs. 2001;19(3):219-27. doi: 10.1023/a:1010608317361.
E7070 is a novel sulfonamide antitumor agent that exhibits potent antitumor activity in vitro and in vivo. This compound affects cell cycle progression in human tumor cells. To elucidate the mechanisms by which E7070 inhibits tumor cell growth, we established and characterized an E7070-resistant subline, A549/ER, from a human non-small cell lung cancer cell line A549. Flow cytometric analyses demonstrated an increase in G0/G1 and a decrease in S phase populations in cells treated with E7070 at 20 or 100 microg/ml for 24 h. Longer exposure to E7070, i.e. 48 and 72 h, increased the G2/M phase fraction in A549 cells. These inhibitory actions of E7070 on cell cycle progression were not observed in A549/ER cells. E7070 inhibited the phosphorylation of pRb, decreased expressions of cyclin A, B1, CDK2, and CDC2 proteins, and suppressed CDK2 catalytic activity with the induction of p53 and p21 proteins in A549 cells but not in A549/ER cells. Taken together, these results suggest that E7070 exerts its antitumor effects by disturbing the cell cycle at multiple points, including both the G1/S and the G2/M transition, in human lung cancer cells.
E7070是一种新型的磺酰胺类抗肿瘤药物,在体外和体内均表现出强大的抗肿瘤活性。该化合物影响人类肿瘤细胞的细胞周期进程。为了阐明E7070抑制肿瘤细胞生长的机制,我们从人非小细胞肺癌细胞系A549中建立并鉴定了一个E7070耐药亚系A549/ER。流式细胞术分析表明,用20或100微克/毫升的E7070处理细胞24小时后,G0/G1期细胞增加,S期细胞减少。对A549细胞延长E7070处理时间,即48和72小时,会增加G2/M期细胞比例。在A549/ER细胞中未观察到E7070对细胞周期进程的这些抑制作用。E7070抑制A549细胞中pRb的磷酸化,降低细胞周期蛋白A、B1、CDK2和CDC2蛋白的表达,并抑制CDK2催化活性,同时诱导p53和p21蛋白,但在A549/ER细胞中未出现这些情况。综上所述,这些结果表明E7070通过在多个点干扰细胞周期,包括G1/S期和G2/M期转换,从而发挥其抗肿瘤作用,作用靶点为人类肺癌细胞。