Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, New York, USA.
J Toxicol Environ Health B Crit Rev. 2011;14(1-4):179-245. doi: 10.1080/10937404.2011.556051.
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.
石棉纤维引发癌症和其他疾病的细胞和分子机制尚未完全阐明。已证实蛇纹石和角闪石石棉纤维均可在体外靶细胞和体内组织中诱导氧化应激、炎症反应、细胞毒性和组织损伤、遗传改变和表观遗传改变。这些机制大多被认为是纤维引起的癌症和非癌性疾病所共有的。本文总结了现有文献中的研究结果,重点关注遗传改变,特别是石棉纤维的致突变性。到目前为止,实验证据表明,突变在石棉致癌性中的作用比石棉引起的纤维化疾病更有说服力。本文从五个方面综述了致突变性对石棉引起的疾病(特别是致癌性)的潜在贡献:(1)纤维诱导的致癌作用中是否存在致突变作用模式(MOA);(2)低剂量的致突变性/致癌性;(3)有助于致突变性的生物学活性以及靶组织/细胞类型的影响;(4)具有或不具有致突变性作为关键事件的健康终点;最后,(5)致突变毒性的决定因素。在本综述的最后,提供了一个已知、被认为是事实但需要确认的以及现有数据空白的共识声明,并提出了未来的研究需求和方向。