tfih是癌细胞新的致命弱点吗?

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Transcription-Austin Pub Date : 2018-01-01 Epub Date: 2017-10-04 DOI:10.1080/21541264.2017.1331723
Pietro Berico, Frédéric Coin
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引用次数: 15

摘要

TFIIH是一个10亚基复合物,参与转录和DNA修复。它含有多种酶活性,包括XPB中atp依赖的DNA转位酶和CDK7中细胞周期蛋白依赖的激酶。最近发现的几种XPB和CDK7抑制剂对许多肿瘤的转录成瘾具有特异性影响,将这些活性确定为癌症化疗的潜在靶点。出乎意料的是,一个参与全局mRNA表达的基础转录因子现在成为了临床上最有希望的癌细胞的致命弱点之一。这些抑制剂也被证明是揭示TFIIH在基因表达中的新功能的有用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Is TFIIH the new Achilles heel of cancer cells?

TFIIH is a 10-subunit complex involved in transcription and DNA repair. It contains several enzymatic activities including a ATP-dependent DNA translocase in XPB and a cyclin-dependent kinase in CDK7. Recently the discovery of several XPB and CDK7 inhibitors with specific impact on the transcriptional addiction of many tumors pinpointed these activities as potential target in cancer chemotherapy. Unexpectedly a basal transcription factor involved in global mRNA expression now emerges a one of the most clinically promising Achilles heels of cancerous cells. These inhibitors also proved to be useful tools to unveil new functions of TFIIH in gene expression.

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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
期刊最新文献
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