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六价铬诱导致癌作用的分子机制。

Molecular mechanisms of Cr(VI)-induced carcinogenesis.

作者信息

Ding Min, Shi Xianglin

机构信息

Pathology and Physiology Research Branch, Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505, USA.

出版信息

Mol Cell Biochem. 2002 May-Jun;234-235(1-2):293-300.

Abstract

Although Cr(VI)-containing compounds are well documented carcinogens, their mechanism of action is still not well understood. Recent studies have suggested that reduction of Cr(VI) to its lower oxidation states and related free radical reactions play an important role in Cr(VI)-induced carcinogenesis. This article summarizes recent studies from our laboratory on (a) the reduction of Cr(VI) by ascorbate, diol- and thiol-containing molecules, certain flavoenzymes, cell organelles, intact cells, and whole animals; (b) free radical production in both non-cellular and cellular systems; and (c) Cr(VI)-induced DNA damage, activation of nuclear transcription factor KB (NF-kappaB), activator protein-1, p53, hypoxia-inducible factor-1, vascular endothelial growth factor, tyrosine phosphorylation, apoptosis, cell growth arrest, and gene expression profile.

摘要

尽管含六价铬的化合物是有充分文献记载的致癌物,但其作用机制仍未完全明确。最近的研究表明,六价铬还原为较低氧化态以及相关的自由基反应在六价铬诱导的致癌过程中起重要作用。本文总结了我们实验室最近关于以下方面的研究:(a)抗坏血酸、含二醇和硫醇的分子、某些黄素酶、细胞器、完整细胞及整体动物对六价铬的还原作用;(b)非细胞和细胞系统中自由基的产生;(c)六价铬诱导的DNA损伤、核转录因子KB(NF-κB)、激活蛋白-1、p53、缺氧诱导因子-1、血管内皮生长因子的激活、酪氨酸磷酸化、细胞凋亡、细胞生长停滞及基因表达谱。

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