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Toxicogenomic Effect of Liver-toxic Environmental Chemicals in Human Hepatoma Cell Line
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  • Toxicogenomic Effect of Liver-toxic Environmental Chemicals in Human Hepatoma Cell Line
  • Toxicogenomic Effect of Liver-toxic Environmental Chemicals in Human Hepatoma Cell Line
저자명
Kim. Seung-Jun,Park. Hye-Won,Yu. So-Yeon,Kim. Jun-Sub,Ha. Jung-Mi,Youn. Jong-Pil,An. Yu-Ri,Oh. Moon-Ju,Kim. Youn-Jung,Ryu. Jae-C
간행물명
Molecular & cellular toxicology
권/호정보
2009년|5권 4호|pp.310-316 (7 pages)
발행정보
대한독성유전단백체학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

Some environmental chemicals have been shown to cause liver-toxicity as the result of bioaccumulation. Particularly, fungicides have been shown to cause varying degrees of hepatictoxicity and to disrupt steroid hormone homeostasis in in vivo models. The principal objective of this study was to evaluate the liver-toxic responses of environmental chemicals-in this case selected fungicides and parasiticides-in order to determine whether or not this agent differentially affected its toxicogenomic activities in hepatic tumor cell lines. To determine the gene expression profiles of 3 fungicides (triadimefon, myclobutanil, vinclozolin) and 1 parasiticide (dibutyl phthalate), we utilized a modified HazChem human array V2. Additionally, in order to observe the differential alterations in its time-dependent activities, we conducted two time (3 hr, 48 hr) exposures to the respective IC20 values of four chemicals. As a result, we analyzed the expression profiles of a total of 1638 genes, and we identified 70 positive significant genes and 144 negative significant genes using four fungicidic and parasiticidic chemicals, using SAM (Significant Analysis of Microarray) methods (q-value<0.5%). These genes were analyzed and identified as being related to apoptosis, stress responses, germ cell development, cofactor metabolism, and lipid metabolism in GO functions and pathways. Additionally, we found 120 genes among those time-dependently differentially expressed genes, using 1-way ANOVA (P-value<0.05). These genes were related to protein metabolism, stress responses, and positive regulation of apoptosis. These data support the conclusion that the four tested chemicals have common toxicogenomic effects and evidence respectively differential expression profiles according to exposure time.