Effect of gnrh analogs on the expression of trka and p75 neurotrophin receptors in primary cell cultures from human prostate adenocarcinoma
Autor: | Christian Huidobro, Dixan A. Benitez, Enrique A. Castellón, Catherine Sánchez, Marisa Clementi, Héctor R. Contreras |
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Jazyk: | angličtina |
Rok vydání: | 2005 |
Předmět: |
Agonist
Male medicine.medical_specialty Antineoplastic Agents Hormonal medicine.drug_class Urology Blotting Western Tetrazolium Salts Apoptosis Receptors Nerve Growth Factor Tropomyosin receptor kinase A Adenocarcinoma Receptor Nerve Growth Factor Gonadotropin-Releasing Hormone Prostate cancer Internal medicine medicine Low-affinity nerve growth factor receptor Humans Receptor trkA skin and connective tissue diseases Receptor Cell Proliferation Formazans biology Reverse Transcriptase Polymerase Chain Reaction Prostatic Neoplasms Epithelial Cells medicine.disease Endocrinology Nerve growth factor nervous system Oncology Cancer cell biology.protein sense organs Comet Assay Leuprolide Neurotrophin |
Zdroj: | PROSTATE Artículos CONICYT CONICYT Chile instacron:CONICYT |
Popis: | BACKGROUND GnRH analogs have antiproliferative and/or apoptotic effects on prostate cancer cells. Also, neurotrophin receptors TrkA and p75 have been reported in normal prostate suggesting a role in the gland growth control. In prostate cancer, TrkA receptors seem to be overexpressed and p75 receptors show a decreased expression. These changes in neurotrophin receptors may be related with unbalanced growth in malignant cells. In the present study we investigate the effects of GnRH analogs (leuprolide and cetrorelix) on the expression of TrkA and p75 neurotrophin receptors in primary cultures of human prostate cancer cells. METHODS Tissue was obtained from radical prostatectomies due to prostate adenocarcinoma. Cells were isolated after sequential enzyme digestion and cultured in defined media. Nerve growth factor (NGF) receptors in untreated cultures were estimated by immunofluorescence. Cultures were treated with leuprolide (agonist) or cetrorelix (antagonist) and expression of TrkA and p75 receptors were evaluated by semi quantitative RT-PCR (polymerase chain reaction) and western blot. Cell proliferation was estimated by MTT method and apoptosis through COMET assay. RESULTS Both leuprolide and cetrorelix induced a significant increase in p75 receptor gene and protein expression at a concentration that induce apoptosis and decrease proliferation. TrkA receptors showed no changes in presence of GnRH analogs. CONCLUSIONS GnRH analogs, leuprolide, and cetrorelix, change the ratio between neurotrophin receptors TrkA and p75 by increasing gene and protein expression of p75 receptor. Considering that TrkA receptor is related with proliferation and p75 with apoptosis, we suggest that our findings may explain, in part, the effect of GnRH analogs on prostate cancer growth. © 2005 Wiley-Liss, Inc. |
Databáze: | OpenAIRE |
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