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去泛素化酶与 DNA 损伤应答通路。

Deubiquitylating enzymes and DNA damage response pathways.

机构信息

MISSION Therapeutics Ltd, Babraham Research Campus, Cambridge, CB22 3AT, UK.

出版信息

Cell Biochem Biophys. 2013 Sep;67(1):25-43. doi: 10.1007/s12013-013-9635-3.

Abstract

Covalent post-translational modification of proteins by ubiquitin and ubiquitin-like factors has emerged as a general mechanism to regulate myriad intra-cellular processes. The addition and removal of ubiquitin or ubiquitin-like proteins from factors has recently been demonstrated as a key mechanism to modulate DNA damage response (DDR) pathways. It is thus, timely to evaluate the potential for ubiquitin pathway enzymes as DDR drug targets for therapeutic intervention. The synthetic lethal approach provides exciting opportunities for the development of targeted therapies to treat cancer: most tumours have lost critical DDR pathways, and thus rely more heavily on the remaining pathways, while normal tissues are still equipped with all DDR pathways. Here, we review key deubiquitylating enzymes (DUBs) involved in DDR pathways, and describe how targeting DUBs may lead to selective therapies to treat cancer patients.

摘要

蛋白质的泛素化和类泛素化的翻译后共价修饰已成为调节多种细胞内过程的通用机制。最近的研究表明,泛素或类泛素蛋白从因子上的添加和去除是调节 DNA 损伤反应 (DDR) 途径的关键机制。因此,评估泛素途径酶作为 DDR 药物靶点进行治疗干预的潜力是及时的。合成致死方法为开发治疗癌症的靶向治疗提供了令人兴奋的机会:大多数肿瘤已经失去了关键的 DDR 途径,因此更加依赖于剩余的途径,而正常组织仍然配备了所有的 DDR 途径。在这里,我们综述了参与 DDR 途径的关键去泛素化酶 (DUBs),并描述了靶向 DUBs 如何可能导致治疗癌症患者的选择性治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bcd/3756857/d0208499bf3d/12013_2013_9635_Fig1_HTML.jpg

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