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真核翻译机制抑制剂作为治疗药物。

Inhibitors of Eukaryotic Translational Machinery as Therapeutic Agents.

机构信息

Department of Discovery Chemistry, Merck & Co., Inc., South San Francisco, California 94080, United States.

出版信息

J Med Chem. 2021 Mar 11;64(5):2436-2465. doi: 10.1021/acs.jmedchem.0c01746. Epub 2021 Feb 16.

Abstract

Inhibiting eukaryotic protein translation with small molecules is emerging as a powerful therapeutic strategy. The advantage of targeting cellular translational machinery is that it is required for the highly proliferative state of many neoplastic cells, replication of certain viruses, and ultimately the expression of a wide variety of protein targets. Although, this approach has been exploited to develop clinical agents, such as homoharringtonine (HHT, ), used to treat chronic myeloid leukemia (CML), inhibiting components of the translational machinery is often associated with cytotoxic phenotypes. However, recent studies have demonstrated that certain small molecules can inhibit the translation of specific subsets of proteins, leading to lower cytotoxicity, and opening-up therapeutic opportunities for translation inhibitors to be deployed in indications beyond oncology and infectious disease. This review summarizes efforts to develop inhibitors of the eukaryotic translational machinery as therapeutic agents and highlights emerging opportunities for translation inhibitors in the future.

摘要

用小分子抑制真核蛋白翻译正在成为一种强大的治疗策略。靶向细胞翻译机制的优势在于,它是许多肿瘤细胞的高度增殖状态、某些病毒的复制以及最终广泛表达各种蛋白质靶标所必需的。尽管这种方法已被用于开发临床制剂,如用于治疗慢性髓性白血病 (CML) 的高三尖杉酯碱 (HHT),但抑制翻译机制的成分通常与细胞毒性表型相关。然而,最近的研究表明,某些小分子可以抑制特定蛋白质亚群的翻译,从而降低细胞毒性,并为翻译抑制剂在肿瘤学和传染病以外的适应症中的应用开辟治疗机会。本文综述了开发真核翻译机制抑制剂作为治疗剂的努力,并强调了翻译抑制剂在未来的新机会。

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