Recent advances of selenized tubulin inhibitors in cancer therapy.

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL
Yong-Chang Zhao, Liang-Qing Yan, Yuan Xu
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引用次数: 0

Abstract

Cancer treatment always a huge challenge amidst the resistance and relapse caused by the various treatments. Inhibitors targeting mitosis have been considered as promising therapeutic drugs in clinic, of which tubulins play an important role. Selenium (Se) as an essential microelement in humans and animals, playing a crucial role in the formation of anti-oxidase (glutathione peroxidase) and selenoprotein, also attracted broad attention in cancer therapy. Because the introduction of Se atom could change the length and angle of chemical bond and alter their functional properties, regulating selenized chemotherapeutics has become one of the hot spots. However, little attention has been paid to studying the combination of Se and tubulin inhibitors. Herein, we review the latest research results of selenized tubulin inhibitors in cancer therapy, including its mechanisms, categories and biological activities, providing a theoretical basis for different selenized microtubules inhibitors therapies.

硒化微管蛋白抑制剂在癌症治疗中的最新进展。
癌症治疗始终是一个巨大的挑战,因为各种治疗方法都会引起抗药性和复发。针对有丝分裂的抑制剂被认为是临床上很有前景的治疗药物,其中管蛋白发挥着重要作用。硒(Se)作为人类和动物必需的微量元素,在抗氧化物酶(谷胱甘肽过氧化物酶)和硒蛋白的形成中发挥着重要作用,在癌症治疗中也引起了广泛关注。由于 Se 原子的引入可改变化学键的长度和角度,从而改变其功能特性,因此硒化化疗药物的调控已成为研究热点之一。然而,人们很少关注 Se 与小管蛋白抑制剂的结合研究。在此,我们综述了硒化微管蛋白抑制剂在癌症治疗中的最新研究成果,包括其机制、类别和生物活性,为不同的硒化微管蛋白抑制剂疗法提供理论依据。
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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来源期刊
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
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