Use of cDNA microarrays to analyze dioxin-induced changes in human liver gene expression

被引:109
作者
Frueh, FW
Hayashibara, KC
Brown, PO
Whitlock, JP
机构
[1] Stanford Univ, Sch Med, Dept Mol Pharmacol, Stanford, CA 95305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Biochem, Stanford, CA 95305 USA
关键词
cDNA microarray; gene expression; gene regulation; liver; dioxin; TCDD;
D O I
10.1016/S0378-4274(01)00364-2
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
One mechanism by which cells adapt to environmental changes is by altering gene expression. Here, we have used cDNA microarrays to identify genes whose expression is altered by exposure to the environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). The goal of our study was to enhance our understanding or toxicity mediated through the pathway by which TCDD stimulates gene expression. To model this toxicity response, we exposed human hepatoma (HepG2) cells to TCDD (10 nM for 18 h) and analyzed mRNA by two-color fluorescent hybridization to cDNA sequences immobilized on glass microscope slides (2.5 x 7.5 cm) covering a surface area of 2.25 cm(2). We analyzed approximately one-third of the genes expressed in HepG2 cells and found that TCDD up- or down-regulates 112 genes two-fold or more. Most changes are relatively subtle (two- to four-fold). We verified the regulation of protooncogene cot, XMP, and human enhancer of filamentation-1 (HEF1), genes involved in cellular proliferation, as well as metallothionein, plasminogen activator inhibitor (PAI1), and HM74, genes involved in cellular signaling and regeneration, To characterize the response in more detail, we performed time-course. dose-dependence studies, and cycloheximide experiments. We observed direct and indirect responses to TCDD implying that adaptation to TCDD (and other related environmental stimuli) is substantially more complex than we previously realized. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:189 / 203
页数:15
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