Hippuristanol - A potent steroid inhibitor of eukaryotic initiation factor 4A.

Translation (Austin, Tex.) Pub Date : 2016-01-04 eCollection Date: 2016-01-01 DOI:10.1080/21690731.2015.1137381
Regina Cencic, Jerry Pelletier
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引用次数: 45

Abstract

Protein synthesis and its regulatory signaling pathways play essential roles in the initiation and maintenance of the cancer phenotype. Insight obtained over the last 3 decades on the mechanisms regulating translation in normal and transformed cells have revealed that perturbed control in cancer cells may offer an Achilles' heel for the development of novel anti-neoplastic agents. Several small molecule inhibitors have been identified and characterized that target translation initiation - more specifically, the rate-limiting step where ribosomes are recruited to mRNA templates. Among these, hippuristanol, a polyhydroxysteroid from the gorgonian Isis hippuris has been found to inhibit translation initiation by blocking the activity of eukaryotic initiation factor (eIF) 4A, an essential RNA helicase involved in this process. Herein, we highlight the biological properties of this compound, its potential development as an anti-cancer agent, and its use to validate eIF4A as an anti-neoplastic target.

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hipuristol -真核起始因子4A的有效类固醇抑制剂。
蛋白质合成及其调控信号通路在癌症表型的启动和维持中发挥重要作用。在过去的30年里,对正常细胞和转化细胞的翻译调节机制的深入研究表明,癌细胞中受干扰的控制可能是开发新型抗肿瘤药物的致命弱点。几种小分子抑制剂已被确定并表征为靶翻译起始-更具体地说,是核糖体被招募到mRNA模板的限速步骤。其中,来自柳柑属Isis hippuris的一种多羟基类固醇hippuristol被发现通过阻断真核起始因子(eIF) 4A的活性来抑制翻译起始,eIF 4A是翻译起始过程中必需的RNA解旋酶。在此,我们重点介绍了该化合物的生物学特性,其作为抗癌药物的潜在发展,以及其用于验证eIF4A作为抗肿瘤靶点的应用。
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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