Targeting Cell Survival Factors, HSF1 and HSPs, with a Specific Inhibitor for Cancer Therapy

K. Ohtsuka
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引用次数: 4

Abstract

It has been known that major heat shock proteins, such as Hsp90 and Hsp70, and their transcription factor HSF1 are overexpressed in a wide range of cancer cells. Its biological significance, however, remains unclear. Recently, it has been recognized that HSF1 and HSPs are cell survival factors and essential for cancer cell development and progression, and the HSF1-HSPs system seems to be co-opted by cancer cells for their own survival under stressful conditions (low oxygen concentration, low nutrient, low pH). According to this conception, targeting HSF1 and HSPs with a specific inhibitor has been suggested for cancer therapy. Hsp90 inhibitors have long been studied from 1990ʼ not only in a basic research but also in clinical phase I, phase II, even phase III trials. Recently, several inhibitors of Hsp70 and HSF1 for the purpose of cancer therapy have been reported. In this review, basic researches aimed for cancer therapy targeting these survival factors (HSF1 and HSPs) with a specific inhibitor are summarized.
靶向细胞生存因子,HSF1和热休克蛋白,用特异性抑制剂治疗癌症
已知主要的热休克蛋白,如Hsp90和Hsp70及其转录因子HSF1在广泛的癌细胞中过表达。然而,其生物学意义尚不清楚。最近,人们已经认识到HSF1和HSPs是细胞生存因子,是癌细胞发育和进展的必要因素,并且HSF1-HSPs系统似乎被癌细胞在应激条件下(低氧浓度、低营养、低pH)的生存所利用。根据这一概念,针对HSF1和热休克蛋白的特异性抑制剂已被建议用于癌症治疗。从1990年开始,Hsp90抑制剂不仅在基础研究中,而且在临床I期、II期甚至III期试验中都得到了广泛的研究。最近,几种Hsp70和HSF1抑制剂被报道用于癌症治疗。本文综述了针对这些生存因子(HSF1和HSPs)的特异性抑制剂治疗癌症的基础研究进展。
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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