Department of Pharmacology and Toxicology, University of Louisville, Louisville, Kentucky 40202.
DNA Repair Section, Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4262.
Toxicol Sci. 2018 Oct 1;165(2):284-290. doi: 10.1093/toxsci/kfy128.
Arsenic is a toxic metalloid widely present in the earth's crust, and is a proven human carcinogen. Chronic arsenic exposure mainly through drinking water causes skin, lung, and urinary bladder cancers, and is associated with liver, prostate, and kidney cancers, cardiovascular and neurological disorders, and diabetes. Several modes of action have been suggested in arsenic carcinogenesis. However, the molecular etiology of arsenic-induced cancer remains unclear. Recent evidence clearly indicates that gene expression modifications induced by arsenic may involve epigenetic alterations, including miRNA dysregulation. Many miRNAs have been implicated in different human cancers as a consequence of losses and or gains of miRNA function that contribute to cancer development. Progress in identifying miRNA dysregulation induced by arsenic has been made using different approaches and models. The present review discusses the recent data regarding dysregulated expression of miRNA in arsenic-induced malignant transformation in vitro, gaps in current understanding and deficiencies in current models for arsenic-induced carcinogenesis, and future directions of research that would improve our knowledge regarding the mechanisms involved in arsenic-induced carcinogenesis.
砷是一种广泛存在于地壳中的有毒类金属,已被证实为人类致癌物。慢性砷暴露主要通过饮用水导致皮肤癌、肺癌和膀胱癌,并与肝癌、前列腺癌和肾癌、心血管和神经紊乱以及糖尿病有关。砷致癌作用的几种作用模式已经被提出。然而,砷诱导癌症的分子病因仍不清楚。最近的证据清楚地表明,砷诱导的基因表达修饰可能涉及表观遗传改变,包括 miRNA 失调。许多 miRNA 已被牵涉到不同的人类癌症中,这是由于 miRNA 功能的丧失和/或获得导致癌症的发展。使用不同的方法和模型,在确定砷诱导的 miRNA 失调方面已经取得了进展。本综述讨论了关于体外砷诱导恶性转化中 miRNA 表达失调的最新数据,目前对砷诱导致癌作用的理解差距和当前模型的缺陷,以及未来的研究方向,这将提高我们对砷诱导致癌作用涉及的机制的认识。