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发展中国家环境镉含量上升:对基因组稳定性和健康的威胁。

Rising environmental cadmium levels in developing countries: threat to genome stability and health.

作者信息

Anetor John I

机构信息

Toxicology/ Micronutrient Metabolism Unit, Department of Chemical Pathology, Faculty of Basic Medical Sciences, College of Medicine, University of Ibadan, Ibadan.

出版信息

Niger J Physiol Sci. 2012 Dec 18;27(2):103-15.

PMID:23652223
Abstract

Cadmium (Cd) is a ubiquitous environmental pollutant of increasing worldwide concern. It is thought to be of greater concern to rapidly industrializing developing countries because of the increasing pace of industrial activities in these countries with increasing consumption and release into the environment. Traditionally, health concerns in exposed human populations have revolved around the association of Cd with bone disease, emphysema and possibly hypertension. Accumulating evidence suggest that Cd is involved in the disruption of many genomic processes, the mechanisms of which are being gradually understood. Changes in DNA Methylation may be induced by cadmium leading to epigenetic alterations. Additionally, though Cd is not thought to induce reactive oxygen species (ROS) directly because it is not capable of accepting or donating electrons under physiological conditions, 8-hydroxy deoxyguanosine (8-OHdG) (a marker of oxidative stress to DNA and a risk factor for cancer among others) has been shown to be elevated in the DNA of testes from rats treated with cadmium chloride, at least in part because Cd inhibits DNA repair mechanisms.  Cadmium is also a metabolic antagonist to Zinc (Zn), an important micronutrient involved in numerous molecular activities. This antagonism alters the physiological stoichiometric relationship between Cd and Zn leading to high Cd/Zn ratio, one consequence of which is high error rate and lack of efficient DNA repair systems leading to high mutation and genome instability culminating in many carcinogenic states, particularly prostate carcinogenesis. Cadmium has also been shown to replace Zn in the tumor suppressor protein, p53 thereby impairing p53's DNA binding activity and associated repair processes. The expression of the p53 protein is significantly depressed by cadmium. Although the rising level of Cd in the environment is widely acknowledged, the occult threat it poses to genome stability largely through inhibition of normal DNA damage repair, oxidative stress and apoptosis and health is poorly recognized. This paper examines the involvement of Cd in the molecular pathways of human disease, providing insight for the prevention of genome instability and associated disease susceptibility particularly cancer across populations through micronutrient intervention, aiding upregulation of the antioxidant defense and DNA repair systems.

摘要

镉(Cd)是一种普遍存在的环境污染物,在全球范围内日益引起关注。由于快速工业化的发展中国家工业活动步伐加快,消费增加且向环境中的排放增多,人们认为这些国家对镉的担忧更为严重。传统上,受镉暴露人群的健康问题主要围绕镉与骨病、肺气肿以及可能的高血压之间的关联。越来越多的证据表明,镉参与了许多基因组过程的破坏,其机制正逐渐被人们所了解。镉可能会诱导DNA甲基化变化,从而导致表观遗传改变。此外,虽然镉在生理条件下不能接受或提供电子,因此不被认为会直接诱导活性氧(ROS),但8-羟基脱氧鸟苷(8-OHdG)(一种DNA氧化应激标志物以及癌症等疾病的风险因素)已被证明在氯化镉处理的大鼠睾丸DNA中含量升高,至少部分原因是镉抑制了DNA修复机制。镉也是锌(Zn)的代谢拮抗剂,锌是一种参与众多分子活动的重要微量营养素。这种拮抗作用改变了镉与锌之间的生理化学计量关系,导致镉/锌比值升高,其后果之一是错误率高且缺乏有效的DNA修复系统,进而导致高突变率和基因组不稳定,最终引发多种致癌状态,尤其是前列腺癌的发生。研究还表明,镉会取代肿瘤抑制蛋白p53中的锌,从而损害p53的DNA结合活性及相关修复过程。镉会显著抑制p53蛋白的表达。尽管环境中镉含量不断上升已得到广泛认可,但它对基因组稳定性造成的潜在威胁,主要是通过抑制正常的DNA损伤修复、氧化应激和细胞凋亡,对健康的影响却鲜为人知。本文探讨了镉在人类疾病分子途径中的作用,通过微量营养素干预,为预防基因组不稳定及相关疾病易感性,尤其是人群中的癌症,提供了思路,有助于上调抗氧化防御和DNA修复系统。

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