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p63的显性负性形式以不依赖p53的方式抑制细胞凋亡。

A dominant negative form of p63 inhibits apoptosis in a p53-independent manner.

作者信息

Lee Hae-ock, Lee Jung-Hwa, Choi Eunhee, Seol Ja Young, Yun Yungdae, Lee Hyunsook

机构信息

Department of Biological Sciences, Research Center for Functional Cellulomics, College of Natural Sciences, Seoul National University, San 56-1 Shillim-dong, Gwanak-ku, Seoul 151-742, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2006 May 26;344(1):166-72. doi: 10.1016/j.bbrc.2006.03.128. Epub 2006 Apr 17.

Abstract

Stem cells are a source of differentiated cells in multiple tissues. If genetic alterations occur in stem cells, the problem persists and malignant cancers may arise. DeltaNp63alpha-a homologue of the tumor suppressor p53-is exclusively expressed in proliferating undifferentiated epithelial cells and cancer cells of epidermal origin. Here, we show that DeltaNp63alpha antagonizes DNA damage-induced apoptosis in a p53-independent manner. We found that upon cellular injury, DeltaNp63alpha must be downregulated before apoptotic program can be activated. The 5637 cell line has abundant levels of DeltaNp63alpha and mutant p53, and it is resistant to DNA damage-induced apoptosis. The knockdown of DeltaNp63alpha by RNA interference sensitized these cells to apoptosis upon genotoxic insult. This suggests that DeltaNp63alpha plays an anti-apoptotic role regardless of the p53 status. Considering the frequent mutations of p53 in tumor cells, our results provide important implications for the treatment of cancers in which p63 is amplified.

摘要

干细胞是多种组织中分化细胞的来源。如果干细胞发生基因改变,问题将持续存在,可能会引发恶性肿瘤。DeltaNp63alpha——肿瘤抑制因子p53的同源物——仅在增殖的未分化上皮细胞和表皮来源的癌细胞中表达。在此,我们表明DeltaNp63alpha以不依赖p53的方式拮抗DNA损伤诱导的细胞凋亡。我们发现,在细胞损伤时,必须下调DeltaNp63alpha才能激活凋亡程序。5637细胞系中DeltaNp63alpha和突变型p53水平丰富,并且对DNA损伤诱导的细胞凋亡具有抗性。通过RNA干扰敲低DeltaNp63alpha可使这些细胞在基因毒性损伤时对细胞凋亡敏感。这表明无论p53状态如何,DeltaNp63alpha都发挥抗凋亡作用。考虑到肿瘤细胞中p53频繁发生突变,我们的结果为治疗p63扩增的癌症提供了重要启示。

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