Abernathy C O, Liu Y P, Longfellow D, Aposhian H V, Beck B, Fowler B, Goyer R, Menzer R, Rossman T, Thompson C, Waalkes M
Division of Cancer Biology, National Cancer Institute, Bethesda, Maryland, USA.
Environ Health Perspect. 1999 Jul;107(7):593-7. doi: 10.1289/ehp.99107593.
A meeting on the health effects of arsenic (As), its modes of action, and areas in need of future research was held in Hunt Valley, Maryland, on 22-24 September 1997. Exposure to As in drinking water has been associated with the development of skin and internal cancers and noncarcinogenic effects such as diabetes, peripheral neuropathy, and cardiovascular diseases. There is little data on specific mechanism(s) of action for As, but a great deal of information on possible modes of action. Although arsenite [As(III)] can inhibit more than 200 enzymes, events underlying the induction of the noncarcinogenic effects of As are not understood. With respect to carcinogenicity, As can affect DNA repair, methylation of DNA, and increase radical formation and activation of the protooncogene c-myc, but none of these potential pathways have widespread acceptance as the principal etiologic event. In addition, there are no accepted models for the study of As-induced carcinogenesis. At the final meeting session we considered research needs. Among the most important areas cited were a) As metabolism and its interaction with cellular constituents; b) possible bioaccumulation of As; c) interactions with other metals; d) effects of As on genetic material; e) development of animal models and cell systems to study effects of As; and f) a better characterization of human exposures as related to health risks. Some of the barriers to the advancement of As research included an apparent lack of interest in the United States on As research; lack of relevant animal models; difficulty with adoption of uniform methodologies; lack of accepted biomarkers; and the need for a central storage repository for stored specimens.
1997年9月22日至24日,一场关于砷(As)对健康的影响、其作用方式以及未来研究需求领域的会议在马里兰州亨特谷举行。饮用水中砷暴露与皮肤癌和内脏癌的发生以及糖尿病、周围神经病变和心血管疾病等非致癌效应有关。关于砷具体的作用机制数据很少,但关于可能的作用方式有大量信息。尽管亚砷酸盐[As(III)]能抑制200多种酶,但砷非致癌效应诱导的潜在机制尚不清楚。关于致癌性,砷可影响DNA修复、DNA甲基化,并增加自由基形成和原癌基因c-myc的激活,但这些潜在途径均未被广泛认可为主要病因事件。此外,目前尚无被广泛接受的砷诱导致癌作用的研究模型。在会议的最后环节,我们审议了研究需求。其中被提及的最重要领域包括:a)砷代谢及其与细胞成分的相互作用;b)砷可能的生物累积;c)与其他金属的相互作用;d)砷对遗传物质的影响;e)开发用于研究砷效应的动物模型和细胞系统;f)更准确地描述与健康风险相关的人类暴露情况。砷研究进展的一些障碍包括:美国对砷研究明显缺乏兴趣;缺乏相关动物模型;难以采用统一方法;缺乏被广泛接受的生物标志物;以及需要一个用于存储标本的中央储存库。