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人p53的温度敏感突变体激活p21WAF1/Cip1表达不会导致细胞凋亡。

Activation of p21WAF1/Cip1 expression by a temperature-sensitive mutant of human p53 does not lead to apoptosis.

作者信息

Kobayashi T, Consoli U, Andreeff M, Shiku H, Deisseroth A B, Zhang W

机构信息

Department of Neuro-Oncology, University of Texas MD Anderson Cancer Center, Houston 77030, USA.

出版信息

Oncogene. 1995 Dec 7;11(11):2311-6.

PMID:8570182
Abstract

The cyclin-dependent kinase inhibitor p21WAF1/Cip1 (p21) inhibits cellular proliferation and has been implicated in p53-dependent apoptosis. In this study, we examined the regulation of p21 in the K562 erythroleukemia cell line using a human temperature-sensitive mutant of p53, 143Ala. We showed that 143Ala at the permissive temperature (32 degrees C) activated the expression of p21. Stable cell lines expressing 143Ala or other p53 mutants were established. We then examined whether elevation of p21 promotes apoptosis and sensitized cells to radiation-induced apoptosis. Our results showed that p21 elevation did not promote or sensitize K562 cells to apoptosis.

摘要

细胞周期蛋白依赖性激酶抑制剂p21WAF1/Cip1(p21)可抑制细胞增殖,并与p53依赖性凋亡有关。在本研究中,我们使用p53的人温度敏感突变体143Ala,检测了K562红白血病细胞系中p21的调控情况。我们发现,在允许温度(32℃)下,143Ala可激活p21的表达。建立了表达143Ala或其他p53突变体的稳定细胞系。然后,我们检测了p21水平的升高是否会促进细胞凋亡,并使细胞对辐射诱导的凋亡敏感。我们的结果表明,p21水平的升高不会促进K562细胞凋亡,也不会使其对凋亡敏感。

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