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Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in Human Prostate and Testicular Cancer
Peroxisome proliferator-activated receptor- [Formula: see text] (PPAR)- [Formula: see text] is a ligand-activated transcriptional factor belonging to steroid receptor superfamily. PPAR- [Formula: see text] plays a role in both adipocyte differentiation and tumorigenesis. Up to date, PPAR- [Formula:...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248699/ https://www.ncbi.nlm.nih.gov/pubmed/18317513 http://dx.doi.org/10.1155/2008/249849 |
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author | Matsuyama, Masahide Yoshimura, Rikio |
author_facet | Matsuyama, Masahide Yoshimura, Rikio |
author_sort | Matsuyama, Masahide |
collection | PubMed |
description | Peroxisome proliferator-activated receptor- [Formula: see text] (PPAR)- [Formula: see text] is a ligand-activated transcriptional factor belonging to steroid receptor superfamily. PPAR- [Formula: see text] plays a role in both adipocyte differentiation and tumorigenesis. Up to date, PPAR- [Formula: see text] is expressed in various cancer tissues, and PPAR- [Formula: see text] ligand induces growth arrest of these cancer cells. In this study, we examined the expression of PPAR- [Formula: see text] in prostate cancer (PC) and testicular cancer (TC) by RT-PCR and immunohistochemistry, and we also examined the effect of PPAR- [Formula: see text] ligand in these cells by MTT assay, hoechest staining, and flow cytometry. PPAR- [Formula: see text] expression was significantly more extensive and intense in malignant tissues than in normal tissues. PPAR- [Formula: see text] ligand induced the reduction of malignant cell viability through apoptosis. These results demonstrated that the generated PPAR- [Formula: see text] in PC and TC cells might play an important role in the tumorigenesis. PPAR- [Formula: see text] may become a new target in the treatment of PC and TC. |
format | Text |
id | pubmed-2248699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22486992008-03-03 Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in Human Prostate and Testicular Cancer Matsuyama, Masahide Yoshimura, Rikio PPAR Res Clinical Study Peroxisome proliferator-activated receptor- [Formula: see text] (PPAR)- [Formula: see text] is a ligand-activated transcriptional factor belonging to steroid receptor superfamily. PPAR- [Formula: see text] plays a role in both adipocyte differentiation and tumorigenesis. Up to date, PPAR- [Formula: see text] is expressed in various cancer tissues, and PPAR- [Formula: see text] ligand induces growth arrest of these cancer cells. In this study, we examined the expression of PPAR- [Formula: see text] in prostate cancer (PC) and testicular cancer (TC) by RT-PCR and immunohistochemistry, and we also examined the effect of PPAR- [Formula: see text] ligand in these cells by MTT assay, hoechest staining, and flow cytometry. PPAR- [Formula: see text] expression was significantly more extensive and intense in malignant tissues than in normal tissues. PPAR- [Formula: see text] ligand induced the reduction of malignant cell viability through apoptosis. These results demonstrated that the generated PPAR- [Formula: see text] in PC and TC cells might play an important role in the tumorigenesis. PPAR- [Formula: see text] may become a new target in the treatment of PC and TC. Hindawi Publishing Corporation 2008 2008-02-19 /pmc/articles/PMC2248699/ /pubmed/18317513 http://dx.doi.org/10.1155/2008/249849 Text en Copyright © 2008 M. Matsuyama and R. Yoshimura. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Matsuyama, Masahide Yoshimura, Rikio Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in Human Prostate and Testicular Cancer |
title | Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in
Human Prostate and Testicular Cancer |
title_full | Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in
Human Prostate and Testicular Cancer |
title_fullStr | Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in
Human Prostate and Testicular Cancer |
title_full_unstemmed | Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in
Human Prostate and Testicular Cancer |
title_short | Peroxisome Proliferator-Activated Receptor- [Formula: see text] Is a Potent Target for Prevention and Treatment in
Human Prostate and Testicular Cancer |
title_sort | peroxisome proliferator-activated receptor- [formula: see text] is a potent target for prevention and treatment in
human prostate and testicular cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248699/ https://www.ncbi.nlm.nih.gov/pubmed/18317513 http://dx.doi.org/10.1155/2008/249849 |
work_keys_str_mv | AT matsuyamamasahide peroxisomeproliferatoractivatedreceptorformulaseetextisapotenttargetforpreventionandtreatmentinhumanprostateandtesticularcancer AT yoshimurarikio peroxisomeproliferatoractivatedreceptorformulaseetextisapotenttargetforpreventionandtreatmentinhumanprostateandtesticularcancer |