Hsp90 Inhibitors are Promising Radiosensitizers for Radiotherapy

N. Kubota, Y. Matsumoto
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引用次数: 1

Abstract

Heat shock protein 90(Hsp90)is an ATP-dependent molecular chaperone protein.The Hsp90 superchaperone complex assists folding and function of a variety of client proteins.Many oncoproteins are Hsp90 client proteins.Compared to normal cels,tumor cels require higher Hsp90 chaperone activity;therefore,targeting Hsp90 with chemical inhibitors disrupts multiple oncogenic processes and has potent antitumor activity.Many Hsp90 inhibitors are currently being tested in preclinical or clinical trials.This review summarizes published data concerning radiosensitization of human tumor cels in in vitro and in vivo tumor models with Hsp90 inhibitors.
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Hsp90抑制剂是有前途的放射治疗增敏剂
热休克蛋白90(Hsp90)是一种atp依赖性分子伴侣蛋白。Hsp90超级伴侣复合物协助多种客户蛋白的折叠和功能。许多癌蛋白是Hsp90客户蛋白。与正常细胞相比,肿瘤细胞需要更高的Hsp90伴侣活性,因此,用化学抑制剂靶向Hsp90可破坏多种致癌过程,具有强大的抗肿瘤活性。许多热休克蛋白90抑制剂目前正在临床前或临床试验中进行测试。本文综述了有关Hsp90抑制剂在体外和体内肿瘤模型中对人肿瘤细胞放射增敏的已发表数据。
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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