Kuroda Junya, Kimura Shinya, Segawa Hidekazu, Sato Kiyoshi, Matsumoto Seiji, Nogawa Masaki, Yuasa Takeshi, Kobayashi Yutaka, Yoshikawa Toshikazu, Ottmann Oliver G, Maekawa Taira
Department of Transfusion Medicine and Cell Therapy, Kyoto University Hospital, Sakyo-ku, Kyoto 606-8507, Japan.
Cancer Sci. 2004 Feb;95(2):186-92. doi: 10.1111/j.1349-7006.2004.tb03202.x.
Zoledronic acid (ZOL), a nitrogen-containing bisphosphonate, exerts anti-tumor effects by inhibiting the prenylation of small GTPases. We have also reported that ZOL shows an anti-leukemic effect by inducing apoptosis throughout the S phase to the G(2) / M boundary. Here, we studied the effects of ZOL on various cell cycle regulators, including p53, cyclin-dependent kinases (CDKs), CDK inhibitors and cyclins, using BV173 leukemia and HCT116 colorectal carcinoma cell lines, harboring wild-type (wt-) p53. ZOL induced the accumulation of neither p53 nor p21(WAF1/CIP1) during the execution of apoptosis in BV173 cells. Therefore, we investigated the dependence of ZOL-induced apoptosis on intact p53 by using wt-p53 HCT116 and a p53-degraded HCT116 subline, and observed no significant difference. p57(KIP2) was upregulated by ZOL in BV173 cells, but not in HCT116 cells. Flow cytometric analyses showed that ZOL also impaired the cell cycle-dependent expression patterns of cyclins A, B and D3 in BV173. In conclusion, the p53-independent anti-tumor activities of ZOL suggest that it may be an attractive agent for treating cancers, including those with chemoresistance resulting from the loss of p53 function. ZOL also affected the coordinate expression patterns of several cell cycle regulators during the execution of anti-tumor activity.
唑来膦酸(ZOL)是一种含氮双膦酸盐,通过抑制小GTP酶的异戊二烯化发挥抗肿瘤作用。我们还报道过ZOL通过诱导整个S期至G(2)/M期边界的细胞凋亡显示出抗白血病作用。在此,我们使用携带野生型(wt-)p53的BV173白血病细胞系和HCT116结肠癌细胞系,研究了ZOL对包括p53、细胞周期蛋白依赖性激酶(CDK)、CDK抑制剂和细胞周期蛋白在内的各种细胞周期调节因子的影响。在BV173细胞凋亡过程中,ZOL既未诱导p53也未诱导p21(WAF1/CIP1)的积累。因此,我们通过使用wt-p53 HCT116和p53降解的HCT116亚系研究了ZOL诱导的凋亡对完整p53的依赖性,未观察到显著差异。ZOL使BV173细胞中的p57(KIP2)上调,但未使HCT116细胞中的p57(KIP2)上调。流式细胞术分析表明,ZOL还破坏了BV173细胞中细胞周期蛋白A、B和D3的细胞周期依赖性表达模式。总之,ZOL不依赖p53的抗肿瘤活性表明它可能是一种有吸引力的治疗癌症的药物,包括那些因p53功能丧失而产生化疗耐药性的癌症。在抗肿瘤活性过程中,ZOL还影响了几种细胞周期调节因子的协同表达模式。