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PMID: 10048147 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Peroxisome proliferator-activated receptors (PPARS) and carcinogenesis.

Vanden Heuvel JP

Abstract

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.

MeSH Terms
Animals Carcinogens/toxicity Gene Expression Regulation Humans Mitogens/toxicity Nuclear Proteins/genetics,physiology Peroxisome Proliferators/toxicity Receptors, Cytoplasmic and Nuclear/genetics,physiology Risk Assessment Transcription Factors/genetics,physiology
Chemicals
Carcinogens Mitogens Nuclear Proteins Peroxisome Proliferators Receptors, Cytoplasmic and Nuclear Transcription Factors
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Vanden Heuvel J P
Department of Veterinary Science, Penn State University, University Park, Pennsylvania 16802, USA. [email protected]
Article Info
Journal
Toxicological sciences : an official journal of the Society of Toxicology
Abbr.
Toxicol Sci
ISSN
1096-6080
Published
1999-01-00
Pages
1-8
Language
English
Region
United States
NLM ID
9805461
Subset
IM
Grants
NIDDK NIH HHS · DK49009 · United States
NIEHS NIH HHS · ES07799 · United States
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