Tao Lianhui, Wang Wei, Li Long, Kramer Paula K, Pereira Michael A
Department of Internal Medicine, Division of Hematology and Oncology, College of Medicine and Public Health, The Ohio State University, Columbus, 43210, USA.
Toxicol Sci. 2005 Oct;87(2):344-52. doi: 10.1093/toxsci/kfi257. Epub 2005 Jul 13.
Bromodichloromethane (BDCM), chloroform, dibromoacetic acid (DBA), dichloroacetic acid (DCA), and trichloroacetic acid (TCA) are chlorine disinfection by-products (DBPs) found in drinking water that have indicated renal carcinogenic and/or tumor promoting activity. We have reported that the DBPs caused DNA hypomethylation in mouse liver, which correlated with their carcinogenic and tumor promoting activity. In this study, we determined their ability to cause renal DNA hypomethylation. B6C3F1 mice were administered DCA or TCA concurrently with/without chloroform in their drinking water for 7 days. In male, but not female mouse kidney, DCA, TCA, and to a lesser extent, chloroform decreased the methylation of DNA and the c-myc gene. Coadministering chloroform increased DCA but not TCA-induced DNA hypomethylation. DBA and BDCM caused renal DNA hypomethylation in both male B6C3F1 mice and Fischer 344 rats. We have reported that, in mouse liver, methionine prevented DCA- and TCA-induced hypomethylation of the c-myc gene. To determine whether it would also prevent hypomethylation in the kidneys, male mice were administered methionine in their diet concurrently with DCA or TCA in their drinking water. Methionine prevented both DCA- and TCA-induced hypomethylation of the c-myc gene. The ability of the DBPs to cause hypomethylation of DNA and of the c-myc gene correlated with their carcinogenic and tumor promoting activity in mouse and rat kidney, which should be taken into consideration as part of their risk assessment. That methionine prevents DCA- and TCA-induced hypomethylation of the c-myc gene would suggest it could prevent their carcinogenic activity in the kidney.
溴二氯甲烷(BDCM)、氯仿、二溴乙酸(DBA)、二氯乙酸(DCA)和三氯乙酸(TCA)是饮用水中发现的氯消毒副产物(DBPs),已表明具有肾致癌和/或肿瘤促进活性。我们曾报道这些消毒副产物会导致小鼠肝脏中的DNA低甲基化,这与其致癌和肿瘤促进活性相关。在本研究中,我们测定了它们导致肾DNA低甲基化的能力。给B6C3F1小鼠的饮用水中同时添加/不添加氯仿给予DCA或TCA,持续7天。在雄性小鼠肾脏中,但雌性小鼠肾脏中未出现,DCA、TCA以及程度较轻的氯仿降低了DNA和c-myc基因的甲基化。同时给予氯仿会增加DCA诱导的DNA低甲基化,但不会增加TCA诱导的DNA低甲基化。DBA和BDCM在雄性B6C3F1小鼠和Fischer 344大鼠的肾脏中均导致DNA低甲基化。我们曾报道,在小鼠肝脏中,蛋氨酸可预防DCA和TCA诱导的c-myc基因低甲基化。为确定其是否也能预防肾脏中的低甲基化,给雄性小鼠在饮食中给予蛋氨酸的同时,在饮用水中给予DCA或TCA。蛋氨酸预防了DCA和TCA诱导的c-myc基因低甲基化。这些消毒副产物导致DNA和c-myc基因低甲基化的能力与其在小鼠和大鼠肾脏中的致癌和肿瘤促进活性相关,在其风险评估中应予以考虑。蛋氨酸可预防DCA和TCA诱导的c-myc基因低甲基化,这表明它可能预防它们在肾脏中的致癌活性。