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异硫氰酸盐在癌症预防中的作用靶点——蛋白质。

Proteins as binding targets of isothiocyanates in cancer prevention.

机构信息

Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20057, USA.

出版信息

Carcinogenesis. 2011 Oct;32(10):1405-13. doi: 10.1093/carcin/bgr111. Epub 2011 Jun 10.

Abstract

Isothiocyanates are versatile cancer-preventive compounds. Evidence from animal studies indicates that the anticarcinogenic activities of ITCs involve all the major stages of tumor growth: initiation, promotion and progression. Epidemiological studies have also shown that dietary intake of ITCs is associated with reduced risk of certain human cancers. A number of mechanisms have been proposed for the chemopreventive activities of ITCs. To identify the molecular targets of ITCs is a first step to understand the molecular mechanisms of ITCs. Studies in recent years have shown that the covalent binding to certain protein targets by ITCs seems to play an important role in ITC-induced apoptosis and cell growth inhibition and other cellular effects. The knowledge gained from these studies may be used to guide future design and screen of better and more efficacious compounds. In this review, we intend to cover all potential protein targets of ITCs so far studied and summarize what are known about their binding sites and the potential biological consequences. In the end, we also offer discussions to shed light onto the relationship between protein binding and reactive oxygen species generation by ITCs.

摘要

异硫氰酸酯是一种多功能的防癌化合物。动物研究的证据表明,ITC 的抗癌活性涉及肿瘤生长的所有主要阶段:启动、促进和进展。流行病学研究还表明,ITC 的饮食摄入与某些人类癌症风险的降低有关。已经提出了许多机制来解释 ITC 的化学预防作用。确定 ITC 的分子靶标是理解 ITC 分子机制的第一步。近年来的研究表明,ITC 与某些蛋白质靶标的共价结合似乎在 ITC 诱导的细胞凋亡和细胞生长抑制以及其他细胞效应中发挥重要作用。从这些研究中获得的知识可用于指导未来更好、更有效的化合物的设计和筛选。在这篇综述中,我们旨在涵盖迄今为止研究过的所有潜在的 ITC 蛋白靶标,并总结有关它们的结合位点和潜在生物学后果的知识。最后,我们还讨论了 ITC 产生的蛋白质结合与活性氧之间的关系。

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Molecular targets of isothiocyanates in cancer: recent advances.异硫氰酸盐在癌症中的分子靶点:最新进展
Mol Nutr Food Res. 2014 Aug;58(8):1685-707. doi: 10.1002/mnfr.201300684. Epub 2014 Feb 10.

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