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靶向癌症中的变构二硫键。

Targeting allosteric disulphide bonds in cancer.

机构信息

Lowy Cancer Research Centre and Prince of Wales Clinical School, University of New South Wales, Sydney NSW 2052, Australia.

出版信息

Nat Rev Cancer. 2013 Jun;13(6):425-31. doi: 10.1038/nrc3519. Epub 2013 May 10.

DOI:10.1038/nrc3519
PMID:23660784
Abstract

Protein action in nature is generally controlled by the amount of protein produced and by chemical modification of the protein, and both are often perturbed in cancer. The amino acid side chains and the peptide and disulphide bonds that bind the polypeptide backbone can be post-translationally modified. Post-translational cleavage or the formation of disulphide bonds are now being identified in cancer-related proteins and it is timely to consider how these allosteric bonds could be targeted for new therapies.

摘要

蛋白质在自然界中的作用通常受到蛋白质产生量和蛋白质化学修饰的控制,而这两者在癌症中通常都会受到干扰。氨基酸侧链以及连接多肽主链的肽键和二硫键可以进行翻译后修饰。在癌症相关蛋白中,现在正在鉴定翻译后切割或二硫键的形成,现在正是考虑如何针对这些变构键开发新疗法的时机。

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Antioxid Redox Signal. 2013 May 20;18(15):1987-2015. doi: 10.1089/ars.2012.4807. Epub 2013 Feb 15.
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Vemurafenib: the first drug approved for BRAF-mutant cancer.威罗菲尼:首个获批准用于 BRAF 突变型癌症的药物。
Comprehensive analysis based on the disulfidptosis-related genes identifies hub genes and immune infiltration for pancreatic adenocarcinoma.
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Identification of disulfidptosis-related genes and immune infiltration in lower-grade glioma.低级别胶质瘤中双硫死亡相关基因的鉴定及免疫浸润
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