Transforming growth factor-β1 coregulates mRNA expression of aryl hydrocarbon receptor and cell-cycle-regulating genes in human cancer cell lines

被引:34
作者
Döhr, O [1 ]
Abel, J [1 ]
机构
[1] Univ Dusseldorf, Dept Toxicol, Med Inst Environm Hyg, D-40225 Dusseldorf, Germany
关键词
D O I
10.1006/bbrc.1997.7773
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming growth factor (TGF)-beta(1) down-regulates mRNA expression of the aryl hydrocarbon receptor (AhR) and of AhR-inducible genes in A549 cells, Here, we describe a dose-dependent inhibition of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-induced cytochrome P450 (CYP) 1A1, CYP1B1 and NADPH-quinone oxidoreductase (NMO-1) mRNA expression as well as TCDD-induced 7-ethoxyresorufin-O-deethylase (EROD) activity in MDA-MB 231 cells. The AhR mRNA expression was not affected by TGF-beta(1). TGF-beta-responsiveness was investigated by examining the effect on the expression of responsive genes, while TGF-beta(1) up-regulates mRNA expression of TGF-beta(1) and TIEG (TGF-beta-inducible early gene) as well as luciferase activity of a responsive reporter plasmid in both cell lines, a down-regulation of c-myc and cyclin A mRNA expression was only found in A549 cells. Furthermore, TGF-beta(1) inhibits only cell proliferation of A549 but not of MDA-MB 231 cells. The results show a coregulation of mRNA expression of AhR and cell-cycle regulating genes, and further indicate that the AhR may be involved in regulation of cell proliferation. (C) 1997 Academic Press.
引用
收藏
页码:86 / 91
页数:6
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