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一种新型抗癌核糖核苷,1-(3-C-乙炔基-β-D-核糖-戊呋喃糖基)胞嘧啶,可增强肿瘤细胞中辐射诱导的细胞死亡。

A novel anticancer ribonucleoside, 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine, enhances radiation-induced cell death in tumor cells.

作者信息

Inanami Osamu, Iizuka Daisuke, Iwahara Akiko, Yamamori Tohru, Kon Yasuhiro, Asanuma Taketoshi, Matsuda Akira, Kashiwakura Ikuo, Kitazato Kenji, Kuwabara Mikinori

机构信息

Laboratory of Radiation Biology, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

Radiat Res. 2004 Dec;162(6):635-45. doi: 10.1667/rr3268.

Abstract

1-(3-C-Ethynyl-beta-D-ribo-pentofuranosyl)cytosine (ECyd, TAS106) is a newly developed anti-tumor agent that targets RNA synthesis. We report here that a low dose of ECyd induces radiosensitization of caspase-dependent apoptosis and reproductive cell death in cells of the gastric tumor cell lines MKN45 and MKN28 and murine rectum adenocarcinoma Colon26. Flow cytometry demonstrated that TAS106 induced the abrogation of the X-ray-induced G(2)/M checkpoint. Western blot analysis showed that X rays increased the expression of cyclin B1, phospho-Cdc2 and Wee1, whereas co-treatment with X rays and TAS106 decreased the expression of these cell cycle proteins associated with the G(2)/M checkpoint. Furthermore, TAS106 was shown to decrease the radiation-induced expression of survivin but not Bcl2 and BclX(L) regardless of TP53 status and cell type. Overexpression of wild-type survivin in MKN45 cells inhibited the induction of apoptosis induced by co-treatment with X rays and TAS106. These results suggest that TAS106 enhances X-ray-induced cell death through down-regulation of survivin and abrogation of the cell cycle machinery.

摘要

1-(3-C-乙炔基-β-D-核糖-呋喃戊糖基)胞嘧啶(ECyd,TAS106)是一种新开发的靶向RNA合成的抗肿瘤药物。我们在此报告,低剂量的ECyd可诱导胃癌细胞系MKN45和MKN28以及小鼠直肠腺癌Colon26细胞中依赖半胱天冬酶的凋亡和生殖细胞死亡的放射增敏作用。流式细胞术表明,TAS106可诱导X射线诱导的G(2)/M期检查点的消除。蛋白质印迹分析表明,X射线可增加细胞周期蛋白B1、磷酸化Cdc2和Wee1的表达,而X射线与TAS106联合处理可降低这些与G(2)/M期检查点相关的细胞周期蛋白的表达。此外,无论TP53状态和细胞类型如何,TAS106均显示可降低辐射诱导的生存素表达,但不影响Bcl2和BclX(L)的表达。在MKN45细胞中过表达野生型生存素可抑制X射线与TAS106联合处理诱导的细胞凋亡。这些结果表明,TAS106通过下调生存素和消除细胞周期机制来增强X射线诱导的细胞死亡。

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