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金属诱导的氧化应激与信号转导。

Metal-induced oxidative stress and signal transduction.

作者信息

Leonard Stephen S, Harris Gabriel K, Shi Xianglin

机构信息

National Institute for Occupational Safety and Health, Pathology and Physiology Research Branch, Health Effects Laboratory Division, 1095 Willowdale Road, MS/2015, Morgantown, WV 26505, USA.

出版信息

Free Radic Biol Med. 2004 Dec 15;37(12):1921-42. doi: 10.1016/j.freeradbiomed.2004.09.010.

Abstract

Occupational and environmental exposures to metals are associated with the development of various cancers. Although carcinogenesis caused by metals has been intensively investigated, the mechanisms of action, especially at the molecular level, are still unclear. Accumulating evidence indicates that reactive oxygen species generated by metals may play an important role in the etiology of disease. This review covers recent advances in (1) metal-induced generation of reactive oxygen species; (2) the receptors, kinases, and nuclear transcription factors affected by metals and metal-induced oxidative stress, including growth factor receptors, src kinase, ras signaling, mitogen-activated protein kinases, the phosphoinositide 3-phosphate/Akt pathway, nuclear transcription factor kappaB, activator protein 1, p53, nuclear factor of activated T cells, and hypoxia-inducible factor 1; and (3) global cellular phenomena (signal transduction, cell cycle regulation, and apoptosis) associated with metal-induced ROS production and gene expression.

摘要

职业和环境中金属暴露与多种癌症的发生有关。尽管金属致癌作用已得到深入研究,但其作用机制,尤其是分子水平的机制仍不清楚。越来越多的证据表明,金属产生的活性氧可能在疾病病因中起重要作用。本综述涵盖了以下方面的最新进展:(1)金属诱导的活性氧生成;(2)受金属和金属诱导的氧化应激影响的受体、激酶和核转录因子,包括生长因子受体、src激酶、ras信号传导、丝裂原活化蛋白激酶、磷酸肌醇3-磷酸/Akt途径、核转录因子κB、活化蛋白1、p53、活化T细胞核因子和缺氧诱导因子1;(3)与金属诱导的活性氧产生和基因表达相关的整体细胞现象(信号转导、细胞周期调控和凋亡)。

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