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本文引用的文献

1
Oral ingestion of hexavalent chromium through drinking water and cancer mortality in an industrial area of Greece--an ecological study.希腊工业区饮用水中六价铬的口服摄入与癌症死亡率——一项生态学研究。
Environ Health. 2011 May 24;10:50. doi: 10.1186/1476-069X-10-50.
2
Mechanisms of metal-induced centrosome amplification.金属诱导中心体扩增的机制。
Biochem Soc Trans. 2010 Dec;38(6):1687-90. doi: 10.1042/BST0381687.
3
Aneuploidy as an early mechanistic event in metal carcinogenesis.非整倍体作为金属致癌作用中的早期机制事件。
Biochem Soc Trans. 2010 Dec;38(6):1650-4. doi: 10.1042/BST0381650.
4
Application of the U.S. EPA mode of action Framework for purposes of guiding future research: a case study involving the oral carcinogenicity of hexavalent chromium.美国环保署作用模式框架在指导未来研究中的应用:以六价铬的口腔致癌性为例的研究
Toxicol Sci. 2011 Jan;119(1):20-40. doi: 10.1093/toxsci/kfq320. Epub 2010 Oct 14.
5
Exposure to hexavalent chromium resulted in significantly higher tissue chromium burden compared with trivalent chromium following similar oral doses to male F344/N rats and female B6C3F1 mice.接触六价铬后,雄性 F344/N 大鼠和雌性 B6C3F1 小鼠经口给予相似剂量后,其组织铬负荷明显高于三价铬。
Toxicol Sci. 2010 Dec;118(2):368-79. doi: 10.1093/toxsci/kfq263. Epub 2010 Sep 15.
6
The genotoxicity of physiological concentrations of chromium (Cr(III) and Cr(VI)) and cobalt (Co(II)): an in vitro study.生理浓度的铬(Cr(III) 和 Cr(VI))和钴(Co(II))的遗传毒性:一项体外研究。
Mutat Res. 2010 Jun 1;688(1-2):53-61. doi: 10.1016/j.mrfmmm.2010.03.008. Epub 2010 Mar 20.
7
Characterization of the metabolic and physiologic response to chromium supplementation in subjects with type 2 diabetes mellitus.探讨 2 型糖尿病患者铬补充后的代谢和生理反应特征。
Metabolism. 2010 May;59(5):755-62. doi: 10.1016/j.metabol.2009.09.023. Epub 2009 Dec 22.
8
Hexavalent chromium is carcinogenic to F344/N rats and B6C3F1 mice after chronic oral exposure.长期经口暴露后,六价铬对F344/N大鼠和B6C3F1小鼠具有致癌性。
Environ Health Perspect. 2009 May;117(5):716-22. doi: 10.1289/ehp.0800208. Epub 2008 Dec 31.
9
Chromium picolinate does not improve key features of metabolic syndrome in obese nondiabetic adults.吡啶甲酸铬不能改善肥胖非糖尿病成年人代谢综合征的关键特征。
Metab Syndr Relat Disord. 2009 Apr;7(2):143-50. doi: 10.1089/met.2008.0048.
10
Impact of inorganic nutrients on maintenance of genomic stability.无机营养物对基因组稳定性维持的影响。
Environ Mol Mutagen. 2009 Jun;50(5):349-60. doi: 10.1002/em.20489.

铬与基因组稳定性。

Chromium and genomic stability.

机构信息

Wise Laboratory of Environmental and Genetic Toxicology, Maine Center for Toxicology and Environmental Health, and Department of Applied Medical Sciences, University of Southern Maine, 96 Falmouth St., Portland, ME 04104, United States.

出版信息

Mutat Res. 2012 May 1;733(1-2):78-82. doi: 10.1016/j.mrfmmm.2011.12.002. Epub 2011 Dec 13.

DOI:10.1016/j.mrfmmm.2011.12.002
PMID:22192535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4138963/
Abstract

Many metals serve as micronutrients which protect against genomic instability. Chromium is most abundant in its trivalent and hexavalent forms. Trivalent chromium has historically been considered an essential element, though recent data indicate that while it can have pharmacological effects and value, it is not essential. There is no data indicating that trivalent chromium promotes genomic stability and, instead may promote genomic instability. Hexavalent chromium is widely accepted as highly toxic and carcinogenic with no nutritional value. Recent data indicate that it causes genomic instability and also has no role in promoting genomic stability.

摘要

许多金属作为微量元素,可防止基因组不稳定。铬有三价和六价两种形式,其中三价铬含量最高。三价铬过去一直被认为是一种必需元素,但最近的数据表明,虽然它可能具有药理作用和价值,但并非必需。没有数据表明三价铬可促进基因组稳定,反而可能促进基因组不稳定。六价铬被广泛认为具有高度毒性和致癌性,且无营养价值。最近的数据表明,它会导致基因组不稳定,也没有促进基因组稳定的作用。