Exploration of small-molecule inhibitors targeting Hsp110 as novel therapeutics.

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Rui Zhao, Congke Zhao, Ruizhe Gao, Qinling Cai, Qianbin Li, Liqing Hu
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引用次数: 0

Abstract

The heat shock protein (HSP) 110 family has a key role as a unique class of molecular chaperones maintaining cellular proteostasis in eukaryotes. Abnormal activation of Hsp110 has been implicated in several diseases. Given its important role in pathogenesis, Hsp110 has become a novel drug target for disease diagnosis and targeted therapy. Thus, targeting Hsp110 or its interactions with client proteins offers new therapeutic approaches. Recent studies of small-molecule inhibitors that target Hsp110 in vitro and in vivo have yielded encouraging results. In this review, we provide an overview of novel therapeutics targeting Hsp110, mainly inhibitors of protein-protein interactions (PPIs), together with a brief discussion of the relevant challenges, opportunities, and future directions.

探索靶向Hsp110的小分子抑制剂作为新的治疗方法。
热休克蛋白(HSP) 110家族作为一类独特的分子伴侣在真核生物中起着维持细胞蛋白质平衡的关键作用。Hsp110的异常激活与几种疾病有关。鉴于其在发病机制中的重要作用,Hsp110已成为疾病诊断和靶向治疗的新型药物靶点。因此,靶向Hsp110或其与客户蛋白的相互作用提供了新的治疗方法。最近在体外和体内对靶向Hsp110的小分子抑制剂的研究已经取得了令人鼓舞的结果。在这篇综述中,我们概述了针对Hsp110的新治疗方法,主要是蛋白质-蛋白质相互作用抑制剂(PPIs),并简要讨论了相关的挑战、机遇和未来方向。
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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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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