Peroxisome Proliferator‐Activated Receptor‐γ Is a Potent Target for Prevention and Treatment in Human Prostate and Testicular Cancer
Author(s) -
Masahide Matsuyama,
Rikio Yoshimura
Publication year - 2008
Publication title -
ppar research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 49
eISSN - 1687-4765
pISSN - 1687-4757
DOI - 10.1155/2008/249849
Subject(s) - carcinogenesis , peroxisome proliferator activated receptor , cancer research , prostate cancer , receptor , cancer , flow cytometry , cancer cell , immunohistochemistry , mtt assay , apoptosis , biology , medicine , chemistry , microbiology and biotechnology , biochemistry
Peroxisome proliferator-activated receptor- γ(PPAR)- γis a ligand-activated transcriptional factor belonging to steroid receptor superfamily. PPAR- γplays a role in both adipocyte differentiation and tumorigenesis. Up to date, PPAR- γis expressed in various cancer tissues, and PPAR- γligand induces growth arrest of these cancer cells. In this study, we examined the expression of PPAR- γin prostate cancer (PC) and testicular cancer (TC) by RT-PCR and immunohistochemistry, and we also examined the effect of PPAR- γligand in these cells by MTT assay, hoechest staining, and flow cytometry. PPAR- γexpression was significantly more extensive and intense in malignant tissues than in normal tissues. PPAR- γligand induced the reduction of malignant cell viability through apoptosis. These results demonstrated that the generated PPAR- γin PC and TC cells might play an important role in the tumorigenesis. PPAR- γmay become a new target in the treatment of PC and TC.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom