Senolytic potential of Hsp90 inhibitors

Sayanti Gupta, C. Pan
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引用次数: 0

Abstract

Hsp90 chaperone is an encouraging target for the development of novel anticancer agents. The failure of Hsp90 inhibitors to get regulatory approval for the treatment of cancer is hindered due to toxicity, cost involved in their development and formulation issues. The inhibitors against this chaperone is also being evaluated in pre-clinical models for the treatment of diseases other than cancer (Alzheimer, malaria, AIDS, etc.). Recently, Hsp90 inhibitors have shown promising senolytic effect, that is helpful in increasing the health and life span of mice. The senolytic property of Hsp90 inhibitors will make them less toxic for use in humans. The review focuses on Hsp90 inhibitors discovered till date as senolytic agents along with their future prospects. Further, the various models used for the evaluation of senolytic effect are also discussed.
热休克蛋白90抑制剂的衰老潜能
Hsp90伴侣蛋白是开发新型抗癌药物的一个令人鼓舞的靶点。由于毒性、开发成本和配方问题,Hsp90抑制剂未能获得癌症治疗的监管批准受到阻碍。针对这种伴侣的抑制剂也正在临床前模型中进行评估,用于治疗癌症以外的疾病(阿尔茨海默病、疟疾、艾滋病等)。近年来,热休克蛋白90抑制剂显示出良好的抗衰老作用,有助于提高小鼠的健康和寿命。热休克蛋白90抑制剂的抗衰老特性使其对人体的毒性较小。本文综述了迄今为止发现的Hsp90抑制剂作为抗衰老药物及其未来前景。此外,还讨论了用于评估衰老效应的各种模型。
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来源期刊
Current Chemical Biology
Current Chemical Biology Medicine-Biochemistry (medical)
CiteScore
1.40
自引率
0.00%
发文量
16
期刊介绍: Current Chemical Biology aims to publish full-length and mini reviews on exciting new developments at the chemistry-biology interface, covering topics relating to Chemical Synthesis, Science at Chemistry-Biology Interface and Chemical Mechanisms of Biological Systems. Current Chemical Biology covers the following areas: Chemical Synthesis (Syntheses of biologically important macromolecules including proteins, polypeptides, oligonucleotides, oligosaccharides etc.; Asymmetric synthesis; Combinatorial synthesis; Diversity-oriented synthesis; Template-directed synthesis; Biomimetic synthesis; Solid phase biomolecular synthesis; Synthesis of small biomolecules: amino acids, peptides, lipids, carbohydrates and nucleosides; and Natural product synthesis).
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