High fat diet reduces the expression of glutathione peroxidase 3 in mouse prostate

Prostate. 2011 Oct 1;71(14):1499-509. doi: 10.1002/pros.21365. Epub 2011 Mar 3.


Background: High fat diets are known to be a risk factor for prostate cancer. In this study, we investigated the effect of high fat diet on mouse prostate gene expression.

Methods: C57BL/6J mice were fed either a control or high fat diet for 12 weeks. Microarray analyses were performed on mouse ventral prostate (VP) and dorsolateral prostate (DLP), followed by canonical pathway analysis and regulatory network identification. mRNA changes were confirmed by real time PCR.

Results: Approximately 2,125, and 1,194 genes responded significantly to the high fat diet in VP, DLP, respectively. Pathways and networks related to oxidative stress, glutathione metabolism, NRF-mediated oxidative stress response and NF-kappaB were all differentially regulated by high fat diet. Glutathione peroxidase 3 (GPx3) mRNA levels were decreased by approximately twofold by high fat diet in all three prostate lobes. In human non-transformed prostate cells (PrSC, PrEC, and BPH-1), cholesterol loading decreased GPx3 expression, and increased H2 O2 levels of culture medium. Troglitazone increased GPx3 expression in three normal prostate cells, and decreased H2 O2 levels. In addition, troglitazone attenuated cholesterol-induced H2 O2 increase. Tissue from prostate cancer biopsies had decreased GPx3 mRNA and its level was inversely related to the Gleason score.

Conclusions: High fat diet alters pathways related to many genes concerned with oxidative stress. GPx3, a gene identified by this analysis, was found to be down-regulated by high fat diet and appears be decreased in human prostate cancers, suggesting that GPx3 may have a possible role in modulating carcinogenesis. Prostate 71:1499-1509, 2011. © 2011 Wiley-Liss, Inc.

Keywords: GPx3; cholesterol; high fat diet; mouse; prostate.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cell Line
  • Chromans / pharmacology
  • Diet, High-Fat*
  • Epithelial Cells / cytology
  • Gene Regulatory Networks / drug effects
  • Gene Regulatory Networks / physiology
  • Glutathione Peroxidase / genetics*
  • Glutathione Peroxidase / metabolism
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Lipid Metabolism / genetics
  • Male
  • Mice, Inbred C57BL
  • Oligonucleotide Array Sequence Analysis
  • Oxidative Stress / physiology
  • Prostate / cytology
  • Prostate / enzymology*
  • Prostatic Neoplasms / epidemiology
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / metabolism
  • RNA, Messenger / metabolism
  • Risk Factors
  • Stromal Cells / cytology
  • Thiazolidinediones / pharmacology
  • Troglitazone


  • Chromans
  • Hypoglycemic Agents
  • RNA, Messenger
  • Thiazolidinediones
  • Gpx3 protein, mouse
  • Glutathione Peroxidase
  • Troglitazone