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转移相关蛋白1抑制p53诱导的细胞凋亡。

Metastasis-associated protein 1 inhibits p53-induced apoptosis.

作者信息

Moon Hyo-Eun, Cheon Hwanju, Lee Myung-Shik

机构信息

Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Kangnam-ku, Seoul 135-710, Korea.

出版信息

Oncol Rep. 2007 Nov;18(5):1311-4.

Abstract

Metastasis-associated protein 1 (MTA1) is highly upregulated in cancer cells with metastatic potential; however, the molecular mechanism by which MTA1 increases the metastatic potential of cancer cells is far from clear. We characterized the functional consequences of MTA1 overexpression on p53-induced apoptosis of cancer cells. MTA1 was associated with p53 in a co-immunoprecipitation assay. MTA1 also had deacetylation activity on p53 in human non-small cell lung cancer cells H1299 and human hepatoma cells SK-Hep1. MTA1 attenuated the transactivation and p21 induction by p53. Moreover, MTA1 expression decreased p53-mediated apoptosis. These results indicate that MTA1 inhibits p53-induced apoptosis by deacetylation of p53, which might be related to the increased metastatic potential of cancer cells with high MTA1 expression.

摘要

转移相关蛋白1(MTA1)在具有转移潜能的癌细胞中高度上调;然而,MTA1增加癌细胞转移潜能的分子机制尚不清楚。我们对MTA1过表达对p53诱导的癌细胞凋亡的功能后果进行了表征。在免疫共沉淀试验中,MTA1与p53相关。MTA1在人非小细胞肺癌细胞H1299和人肝癌细胞SK-Hep1中也对p53具有去乙酰化活性。MTA1减弱了p53的反式激活和p21诱导。此外,MTA1表达降低了p53介导的细胞凋亡。这些结果表明,MTA1通过使p53去乙酰化来抑制p53诱导的细胞凋亡,这可能与高MTA1表达的癌细胞转移潜能增加有关。

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