ROLE OF MUTAGENICITY IN ASBESTOS FIBER-INDUCED CARCINOGENICITY AND OTHER DISEASES

被引:118
|
作者
Huang, Sarah X. L. [2 ]
Jaurand, Marie-Claude [3 ]
Kamp, David W. [4 ]
Whysner, John [2 ]
Hei, Tom K. [1 ,2 ]
机构
[1] Columbia Univ, Ctr Radiol Res, Coll Phys & Surg, Dept Radiat Oncol, New York, NY 10032 USA
[2] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
[3] INSERM, Inst Natl Sante & Rech Med, Paris, France
[4] Northwestern Univ, Feinberg Sch Med, Jesse Brown VA Med Ctr, Chicago, IL 60611 USA
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART B-CRITICAL REVIEWS | 2011年 / 14卷 / 1-4期
基金
美国国家卫生研究院;
关键词
PLEURAL MESOTHELIAL CELLS; MADE VITREOUS FIBERS; SINGLE-STRAND BREAKS; LUNG EPITHELIAL-CELLS; HUMAN-MALIGNANT MESOTHELIOMA; SISTER-CHROMATID EXCHANGES; SUPPRESSOR GENE ALTERATIONS; RATS FOLLOWING INOCULATION; STANDARD REFERENCE SAMPLES; INDUCED LIPID-PEROXIDATION;
D O I
10.1080/10937404.2011.556051
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The cellular and molecular mechanisms of how asbestos fibers induce cancers and other diseases are not well understood. Both serpentine and amphibole asbestos fibers have been shown to induce oxidative stress, inflammatory responses, cellular toxicity and tissue injuries, genetic changes, and epigenetic alterations in target cells in vitro and tissues in vivo. Most of these mechanisms are believe to be shared by both fiber-induced cancers and noncancerous diseases. This article summarizes the findings from existing literature with a focus on genetic changes, specifically, mutagenicity of asbestos fibers. Thus far, experimental evidence suggesting the involvement of mutagenesis in asbestos carcinogenicity is more convincing than asbestos-induced fibrotic diseases. The potential contributions of mutagenicity to asbestos-induced diseases, with an emphasis on carcinogenicity, are reviewed from five aspects: (1) whether there is a mutagenic mode of action (MOA) in fiber-induced carcinogenesis; (2) mutagenicity/carcinogenicity at low dose; (3) biological activities that contribute to mutagenicity and impact of target tissue/cell type; (4) health endpoints with or without mutagenicity as a key event; and finally, (5) determinant factors of toxicity in mutagenicity. At the end of this review, a consensus statement of what is known, what is believed to be factual but requires confirmation, and existing data gaps, as well as future research needs and directions, is provided.
引用
收藏
页码:179 / 245
页数:67
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