Peroxisome proliferator-activated receptors (PPARS) and carcinogenesis

被引:75
作者
Vanden Heuvel, JP [1 ]
机构
[1] Penn State Univ, Dept Vet Sci, University Pk, PA 16802 USA
[2] Penn State Univ, Ctr Mol Toxicol, University Pk, PA 16802 USA
关键词
peroxisome proliferators (PP); peroxisome proliferator-activated receptors (PPAR); hepatic mitogens; rats;
D O I
10.1093/toxsci/47.1.1
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Peroxisome proliferators (PPs) are an important group of chemicals that include certain hypolipidemic drugs, plasticizers and pollutants. Many of these agents are known rodent liver tumor promoters and debate exists as to whether humans are at increased cancer risk following exposure to PPs. Research over the last decade has focused on determining the biochemical and molecular mechanisms by which peroxisome proliferators exert their effects, in the hope that this controversy will be settled. PPs regulate gene expression via a steroid hormone receptor, the peroxisome proliferator-activated receptor (PPAR). At least three subtypes of PPAR (alpha, beta and gamma) have been cloned from several species, including humans. These receptors have been implicated in tumor promotion, cellular differentiation, and apoptosis. In the present article, the current understanding of how PPARs are involved in tumorigenesis, and what this may mean to human risk assessment, will be discussed.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 73 条
[1]   PPAR gamma induces cell cycle withdrawal: inhibition of E2F/DP DNA-binding activity via down-regulation of PP2A [J].
Altiok, S ;
Xu, M ;
Spiegelman, BM .
GENES & DEVELOPMENT, 1997, 11 (15) :1987-1998
[2]   Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα) [J].
Aoyama, T ;
Peters, JM ;
Iritani, N ;
Nakajima, T ;
Furihata, K ;
Hashimoto, T ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5678-5684
[3]   MECHANISTICALLY-BASED HUMAN HAZARD ASSESSMENT OF PEROXISOME PROLIFERATOR-INDUCED HEPATOCARCINOGENESIS [J].
ASHBY, J ;
BRADY, A ;
ELCOMBE, CR ;
ELLIOTT, BM ;
ISHMAEL, J ;
ODUM, J ;
TUGWOOD, JD ;
KETTLE, S ;
PURCHASE, IFH .
HUMAN & EXPERIMENTAL TOXICOLOGY, 1994, 13 :S1-S117
[4]   Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans - No alteration in adipose tissue of obese and NIDDM patients [J].
Auboeuf, D ;
Rieusset, J ;
Fajas, L ;
Vallier, P ;
Frering, V ;
Riou, JP ;
Staels, P ;
Auwerx, J ;
Laville, M ;
Vidal, H .
DIABETES, 1997, 46 (08) :1319-1327
[5]   DELAYED-EFFECTS OF CIPROFIBRATE ON RAT-LIVER PEROXISOMAL PROPERTIES AND PROTOONCOGENE EXPRESSION [J].
BARDOT, O ;
CLEMENCET, MC ;
CHERKAOUIMALKI, M ;
LATRUFFE, N .
BIOCHEMICAL PHARMACOLOGY, 1995, 50 (07) :1001-1006
[6]   SUPPRESSION OF LIVER-CELL APOPTOSIS IN-VITRO BY THE NONGENOTOXIC HEPATOCARCINOGEN AND PEROXISOME PROLIFERATOR NAFENOPIN [J].
BAYLY, AC ;
ROBERTS, RA ;
DIVE, C .
JOURNAL OF CELL BIOLOGY, 1994, 125 (01) :197-203
[7]  
Belury M.A., 1997, NUTR DIS UPDATE, V1, P58
[8]   Comparison of dose-response relationships for induction of lipid metabolizing and growth regulatory genes by peroxisome proliferators in rat liver [J].
Belury, MA ;
Moya-Camarena, SY ;
Sun, H ;
Snyder, E ;
Davis, JW ;
Cunningham, ML ;
Vanden Heuvel, JP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 151 (02) :254-261
[9]   Dietary conjugated linoleic acid induces peroxisome-specific enzyme accumulation and ornithine decarboxylase activity in mouse liver [J].
Belury, MA ;
MoyaCamarena, SY ;
Liu, KL ;
Heuvel, JPV .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 1997, 8 (10) :579-584
[10]   HEPATIC PEROXISOME PROLIFERATION IN RODENTS AND ITS SIGNIFICANCE FOR HUMANS [J].
BENTLEY, P ;
CALDER, I ;
ELCOMBE, C ;
GRASSO, P ;
STRINGER, D ;
WIEGAND, HJ .
FOOD AND CHEMICAL TOXICOLOGY, 1993, 31 (11) :857-907