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Updated: Apr 13, 2026

An Orthotopic Murine Model of Human Prostate Cancer Metastasis
Published on: September 18, 2013
Expression of Peroxisome Proliferator Activated Receptor gamma in Prostatic Adenocarcinoma
Hyung Kyu Park1, HyunKyung Kim1, Hyeong-Gon Kim2
1Department of Pathology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea.
Abstract:
Peroxisome proliferator-activated receptor gamma (PPAR-γ), a ligand-activated transcription factor has been investigated as the target for cancer treatment as well as metabolic disorders. Recent studies have demonstrated that PPAR-γ ligands are anti-tumorigenic in prostate cancer due to anti-proliferative and pro-differentiation effects. The aim of this study was to validate PPAR-γ expression in malignant and benign prostate tissues by immunohistochemistry and quantitative real-time polymerase chain reaction (PCR). A total of 730 prostatic adenocarcinomas (PCAs) including 63 whole sections from radical prostatectomy specimens and tissue microarrays containing 667 PCAs were subject to immunostaining for two PPAR-γ antibodies. Twenty-five benign prostate tissues and PCAs were selected for investigating mRNA expression by quantitative real-time PCR. 10.7% of PCAs (78/730) showed cytoplasmic immunoreactivity of PPAR-γ and no nuclear immunoreactivity was noted in PCAs. Most benign prostatic glands showed negative immunoreactivity of PPAR-γ except for variable weak cytoplasmic staining in some glands. Nuclear immunoreactivity of PPAR-γ was noted some central zone and verumontanum mucosal epithelium. The constitutive PPAR-γ mRNA showed significantly lower level in PCAs compared to that in the benign tissues. There was no difference of PPAR-γ mRNA expression between low (≤7) and high (>7) Gleason score groups. There was no association of PPAR-γ mRNA level or cytoplasmic immunostaining with Gleason grade or pathologic stage. Our study supported the evidence of extra-nuclear localization and nongenomic actions of PPAR-γ. Further studies are needed to assess the functional role of PPAR-γ and to validate its therapeutic implication in prostate cancer.
Insights
Peroxisome proliferator-activated receptor gamma (PPAR-γ) expression is reduced in prostate cancer tissues, with primarily cytoplasmic localization observed. This suggests potential non-genomic roles for PPAR-γ in prostate cancer development.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Peroxisome proliferator-activated receptor gamma (PPAR-γ) is a transcription factor implicated in cancer and metabolic disorders.
- PPAR-γ ligands exhibit anti-tumorigenic properties in prostate cancer, showing anti-proliferative and pro-differentiation effects.
Purpose of the Study:
- To validate PPAR-γ expression in malignant and benign prostate tissues using immunohistochemistry and quantitative real-time PCR.
- To investigate the localization and expression levels of PPAR-γ in prostate adenocarcinoma.
Main Methods:
- Immunohistochemistry was performed on 730 prostate adenocarcinomas (PCAs) and 25 benign prostate tissues using two PPAR-γ antibodies.
- Quantitative real-time PCR was used to assess PPAR-γ mRNA expression in a subset of benign and malignant prostate tissues.
- Analysis correlated PPAR-γ expression with Gleason score, pathologic stage, and tissue type.
Main Results:
- Cytoplasmic PPAR-γ immunoreactivity was observed in 10.7% of PCAs, with no nuclear immunoreactivity detected in malignant tissues.
- Benign prostate tissues showed predominantly negative PPAR-γ immunoreactivity, with some weak cytoplasmic staining and nuclear staining in specific epithelial regions.
- Constitutive PPAR-γ mRNA levels were significantly lower in PCAs compared to benign tissues.
- No significant association was found between PPAR-γ mRNA levels or cytoplasmic staining and Gleason score, grade, or pathologic stage.
Conclusions:
- The study supports evidence for extra-nuclear localization and potential non-genomic actions of PPAR-γ in prostate cancer.
- Reduced PPAR-γ expression in prostate cancer suggests a potential role in tumorigenesis.
- Further research is warranted to elucidate the functional role and therapeutic implications of PPAR-γ in prostate cancer.
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