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Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression
Prostate proliferation is dependent of androgens and many peptide hormones. Recent reports suggest that SSTR2 and SHP-1 were two fundamental components on antiproliferative effect of somatostatin. Many studies on SHP-1 revealed that the expression of this protein was diminished or abolished in sever...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667939/ https://www.ncbi.nlm.nih.gov/pubmed/19365586 http://dx.doi.org/10.1155/2009/723831 |
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author | Cariaga-Martinez, Ariel Ernesto Lorenzati, María Angelica Riera, Mario Alejandro Cubilla, Marisa Angelica De La Rossa, Andrés Giorgio, Ernesto Martín Tiscornia, María Mercedes Gimenez, Esteban Mariano Rojas, María Eugenia Chaneton, Bárbara Julieta Rodríguez, Dora Isabel Zapata, Pedro Darío |
author_facet | Cariaga-Martinez, Ariel Ernesto Lorenzati, María Angelica Riera, Mario Alejandro Cubilla, Marisa Angelica De La Rossa, Andrés Giorgio, Ernesto Martín Tiscornia, María Mercedes Gimenez, Esteban Mariano Rojas, María Eugenia Chaneton, Bárbara Julieta Rodríguez, Dora Isabel Zapata, Pedro Darío |
author_sort | Cariaga-Martinez, Ariel Ernesto |
collection | PubMed |
description | Prostate proliferation is dependent of androgens and many peptide hormones. Recent reports suggest that SSTR2 and SHP-1 were two fundamental components on antiproliferative effect of somatostatin. Many studies on SHP-1 revealed that the expression of this protein was diminished or abolished in several of the cancer cell lines and tissues examined. However, it is necessary to confront the cell lines data with real situation in cancer cases. Our studies have shown that epithelial expressions of both proteins, SHP-1 and SSTR2, in normal and benign hyperplasia are localized in the luminal side of duct and acinar cells. Also, SSTR2 is expressed in stromal cells. In malignant prostate tissue, SHP-1 was diminished in 28/45 cases or absent in 12/45 cases, whereas SSTR2 epithelial was diminished in 38/45 cases or lost in only 2/45 cases. The intensity of immunostained was highly negative correlated with Gleason grade for two proteins. |
format | Text |
id | pubmed-2667939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-26679392009-04-13 Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression Cariaga-Martinez, Ariel Ernesto Lorenzati, María Angelica Riera, Mario Alejandro Cubilla, Marisa Angelica De La Rossa, Andrés Giorgio, Ernesto Martín Tiscornia, María Mercedes Gimenez, Esteban Mariano Rojas, María Eugenia Chaneton, Bárbara Julieta Rodríguez, Dora Isabel Zapata, Pedro Darío Adv Urol Research Article Prostate proliferation is dependent of androgens and many peptide hormones. Recent reports suggest that SSTR2 and SHP-1 were two fundamental components on antiproliferative effect of somatostatin. Many studies on SHP-1 revealed that the expression of this protein was diminished or abolished in several of the cancer cell lines and tissues examined. However, it is necessary to confront the cell lines data with real situation in cancer cases. Our studies have shown that epithelial expressions of both proteins, SHP-1 and SSTR2, in normal and benign hyperplasia are localized in the luminal side of duct and acinar cells. Also, SSTR2 is expressed in stromal cells. In malignant prostate tissue, SHP-1 was diminished in 28/45 cases or absent in 12/45 cases, whereas SSTR2 epithelial was diminished in 38/45 cases or lost in only 2/45 cases. The intensity of immunostained was highly negative correlated with Gleason grade for two proteins. Hindawi Publishing Corporation 2009 2009-04-12 /pmc/articles/PMC2667939/ /pubmed/19365586 http://dx.doi.org/10.1155/2009/723831 Text en Copyright © 2009 Ariel Ernesto Cariaga-Martinez et al. 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 | Research Article Cariaga-Martinez, Ariel Ernesto Lorenzati, María Angelica Riera, Mario Alejandro Cubilla, Marisa Angelica De La Rossa, Andrés Giorgio, Ernesto Martín Tiscornia, María Mercedes Gimenez, Esteban Mariano Rojas, María Eugenia Chaneton, Bárbara Julieta Rodríguez, Dora Isabel Zapata, Pedro Darío Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title | Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title_full | Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title_fullStr | Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title_full_unstemmed | Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title_short | Tumoral Prostate Shows Different Expression Pattern of Somatostatin Receptor 2 (SSTR2) and Phosphotyrosine Phosphatase SHP-1 (PTPN6) According to Tumor Progression |
title_sort | tumoral prostate shows different expression pattern of somatostatin receptor 2 (sstr2) and phosphotyrosine phosphatase shp-1 (ptpn6) according to tumor progression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667939/ https://www.ncbi.nlm.nih.gov/pubmed/19365586 http://dx.doi.org/10.1155/2009/723831 |
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