Sano Yuri, Nakashima Hiroshi, Yoshioka Noriyuki, Etho Norihito, Nomiyama Tetsuo, Nishiwaki Yuji, Takebayashi Toru, Oame Kazuyuki
Department of Preventive Medicine and Public Health, Keio University School of Medicine, Tokyo, Japan.
Arch Toxicol. 2009 Sep;83(9):835-49. doi: 10.1007/s00204-009-0431-1. Epub 2009 May 16.
Trichloroethylene (TCE), an industrial organic solvent found in the environment, is a known carcinogen in laboratory animals and is believed to be carcinogenic in humans. Its carcinogenicity is subject to species-specific differences in biological activity, causing hepatocellular carcinoma in mouse and renal-cell carcinoma in rat. We have sought to better understand TCE's mode of action (MOA) by studying the alterations in gene expression profiles of liver in mice and rats that were administrated TCE by oral gavage either once or daily for 14 days. Microarray analysis revealed distinct transcriptional profiles and differences in biological pathways not only species-specific, but also pulse-dose effects within each species. For example, inhibition of the TGF-beta pathway and activation of MAPK signaling were specific to mice repeatedly exposed to TCE. A better understanding of the MOA in mice and rats will lead to better hypotheses of TCE's affect on humans.
三氯乙烯(TCE)是一种存在于环境中的工业有机溶剂,在实验动物中它是一种已知的致癌物,并且被认为对人类也具有致癌性。其致癌性存在生物活性方面的物种特异性差异,可导致小鼠患肝细胞癌以及大鼠患肾细胞癌。我们试图通过研究经口灌胃给予TCE一次或每日给药14天的小鼠和大鼠肝脏基因表达谱的变化,来更好地理解TCE的作用模式(MOA)。微阵列分析揭示了不仅存在物种特异性,而且在每个物种内也存在脉冲剂量效应的独特转录谱和生物途径差异。例如,TGF-β途径的抑制和MAPK信号的激活是反复暴露于TCE的小鼠所特有的。对小鼠和大鼠作用模式的更好理解将有助于提出关于TCE对人类影响的更好假设。