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生长抑制家族蛋白5的截短可有效诱导人舌鳞状细胞癌细胞系衰老,但不会诱导其凋亡。

Truncation of inhibitor of growth family protein 5 effectively induces senescence, but not apoptosis in human tongue squamous cell carcinoma cell line.

作者信息

Qi Lin, Zhang Yang

机构信息

Department of Orthodontics, School of Stomatology, China Medical University, Shenyang, Liaoning, China.

出版信息

Tumour Biol. 2014 Apr;35(4):3139-44. doi: 10.1007/s13277-013-1410-y. Epub 2013 Nov 20.

Abstract

In these studies, inhibitor of growth protein 5 (ING5) and various fragments of it were overexpressed in the human tongue squamous cell carcinoma cell line, HSC-3. The roles of ING5 in HSC-3 cells were then identified in vitro. Our results indicate that intact ING5 can inhibit proliferation and induce apoptosis in HSC-3 cells. Moreover, two truncated fragments of ING5 (aa 1-184 and aa 107-226) can induce cellular senescence. To analyze the signaling pathway involved, western blotting was performed. In these assays, two truncated fragments of ING5 were found to inhibit the cyclin E and CDK2 expression. These results are consistent with the S phase arrest observed with the overexpression of truncated ING5. However, the mechanisms of ING5-induced cellular senescence remain unclear, and extensive investigations are required in future studies.

摘要

在这些研究中,生长抑制蛋白5(ING5)及其各种片段在人舌鳞状细胞癌细胞系HSC-3中过表达。然后在体外确定ING5在HSC-3细胞中的作用。我们的结果表明,完整的ING5可以抑制HSC-3细胞的增殖并诱导其凋亡。此外,ING5的两个截短片段(氨基酸1-184和氨基酸107-226)可诱导细胞衰老。为了分析所涉及的信号通路,进行了蛋白质印迹分析。在这些试验中,发现ING5的两个截短片段可抑制细胞周期蛋白E和CDK2的表达。这些结果与截短的ING5过表达所观察到的S期阻滞一致。然而,ING5诱导细胞衰老的机制仍不清楚,未来的研究需要进行广泛的调查。

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