Role of the aryl hydrocarbon receptor in cell cycle regulation

被引:56
作者
Puga, A
Marlowe, J
Barnes, S
Chang, CY
Maier, A
Tan, ZQ
Kerzee, JK
Chang, XQ
Strobeck, M
Knudsen, ES
机构
[1] Univ Cincinnati, Med Ctr, Dept Environm Hlth, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Med Ctr, Dept Cell Biol Neurobiol & Anat, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Med Ctr, Ctr Environm Genet, Cincinnati, OH 45267 USA
关键词
aromatic hydrocarbon receptor; retinoblastoma; protein interactions; cell cycle; E2F; environmental sensors;
D O I
10.1016/S0300-483X(02)00276-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the most puzzling aspects of the biological impact of polycyclic aromatic hydrocarbon compounds is that they elicit an apparently unrelated variety of toxic, teratogenic, and carcinogenic responses in exposed animals and in humans. At the cellular level, these environmental toxicants affect cell cycle regulatory mechanisms and signal transduction pathways in ways that are equally diverse and often contradictory. For example, depending on the particular cell lines studied, exposure to these compounds may lead to cell proliferation, to terminal differentiation, or to apoptosis. These effects are mediated by the aryl hydrocarbon receptor, a ligand-activated transcription factor well known for its regulatory activity on the expression of several phase I detoxification cytochrome P450 genes. Research into the molecular mechanisms of aryl hydrocarbon receptor function has uncovered a novel role for this protein during cell cycle progression. The activated receptor acts as an environmental sensor and cell cycle checkpoint that commits cells exposed to adverse environmental stimuli to arrest before the onset of DNA replication. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:171 / 177
页数:7
相关论文
共 51 条
[1]   Review of the interaction between TCDD and glucocorticoids in embryonic palate [J].
Abbott, BD .
TOXICOLOGY, 1995, 105 (2-3) :365-373
[2]   THE MECHANISM OF DIOXIN TOXICITY - RELATIONSHIP TO RISK ASSESSMENT [J].
BIRNBAUM, LS .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :157-167
[3]   PARTIAL DEMASCULINIZATION AND FEMINIZATION OF SEX BEHAVIOR IN MALE-RATS BY IN-UTERO AND LACTATIONAL EXPOSURE TO 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN IS NOT ASSOCIATED WITH ALTERATIONS IN ESTROGEN-RECEPTOR BINDING OR VOLUMES OF SEXUALLY DIFFERENTIATED BRAIN NUCLEI [J].
BJERKE, DL ;
BROWN, TJ ;
MACLUSKY, NJ ;
HOCHBERG, RB ;
PETERSON, RE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1994, 127 (02) :258-267
[4]   INDUCTION OF HIGHLY PROLIFERATIVE PHENOTYPES IN CULTURED GLOMERULAR MESANGIAL CELLS BY BENZO[A]PYRENE ALONE OR IN COMBINATION WITH METHOXAMINE [J].
BOWES, RC ;
WEBER, TJ ;
RAMOS, KS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 323 (02) :243-250
[5]   CLONING OF THE AH-RECEPTOR CDNA REVEALS A DISTINCTIVE LIGAND-ACTIVATED TRANSCRIPTION FACTOR [J].
BURBACH, KM ;
POLAND, A ;
BRADFIELD, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8185-8189
[6]  
Carver LA, 1997, J BIOL CHEM, V272, P11452
[7]   Constitutive activation of the aromatic hydrocarbon receptor [J].
Chang, CY ;
Puga, A .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (01) :525-535
[8]  
CHOI EJ, 1991, J BIOL CHEM, V266, P9591
[9]   DIOXINS - MODEL CHEMICALS FOR ASSESSING RECEPTOR-MEDIATED TOXICITY [J].
DEVITO, MJ ;
BIRNBAUM, LS .
TOXICOLOGY, 1995, 102 (1-2) :115-123
[10]  
DOLWICK KM, 1993, MOL PHARMACOL, V44, P911