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微管活性药物紫杉醇、长春碱和诺考达唑可提高转录活性p53的水平。

Microtubule-active drugs taxol, vinblastine, and nocodazole increase the levels of transcriptionally active p53.

作者信息

Tishler R B, Lamppu D M, Park S, Price B D

机构信息

Joint Center for Radiation Therapy, Boston, Massachusetts 02115, USA.

出版信息

Cancer Res. 1995 Dec 15;55(24):6021-5.

PMID:8521385
Abstract

A range of DNA-damaging agents has been shown to increase cellular levels of the nuclear phosphoprotein p53 and to induce p53-dependent processes. We examined the ability of three microtubule-active agents, taxol, vinblastine, and nocodazole, to increase p53 levels and activate p53-dependent processes. When tested using a p53 DNA-binding assay, all three agents induced p53 in a dose-dependent manner. To varying degrees, these agents also induced p21WAF1/CIP1 mRNA and transcription in a chloramphenicol acetyl transferase reporter system. These data suggest there is an additional pathway for activating p53 and subsequent p53-dependent processes.

摘要

一系列DNA损伤剂已被证明可提高细胞核磷蛋白p53的细胞水平,并诱导p53依赖性过程。我们研究了三种微管活性剂紫杉醇、长春碱和诺考达唑提高p53水平并激活p53依赖性过程的能力。当使用p53 DNA结合试验进行测试时,所有这三种试剂均以剂量依赖性方式诱导p53。在氯霉素乙酰转移酶报告系统中,这些试剂还不同程度地诱导了p21WAF1/CIP1 mRNA和转录。这些数据表明,存在激活p53及随后的p53依赖性过程的另一条途径。

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