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Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer
INTRODUCTION AND OBJECTIVE: Overexpression of MMPs has been related to biochemical recurrence after radical prostatectomy. TIMP1 and TIMP2 are controllers of MMPs and the aim of this study is to evaluate the expression levels of MMPs and their regulators using immunohistochemistry in tissue microarr...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756933/ https://www.ncbi.nlm.nih.gov/pubmed/26742965 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0451 |
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author | dos Reis, Sabrina Thalita Viana, Nayara Izabel Iscaife, Alexandre Pontes, José Dip, Nelson Antunes, Alberto Azoubel Guimarães, Vanessa Ribeiro Santana, Isaque Nahas, William Carlos Srougi, Miguel Leite, Katia Ramos Moreira |
author_facet | dos Reis, Sabrina Thalita Viana, Nayara Izabel Iscaife, Alexandre Pontes, José Dip, Nelson Antunes, Alberto Azoubel Guimarães, Vanessa Ribeiro Santana, Isaque Nahas, William Carlos Srougi, Miguel Leite, Katia Ramos Moreira |
author_sort | dos Reis, Sabrina Thalita |
collection | PubMed |
description | INTRODUCTION AND OBJECTIVE: Overexpression of MMPs has been related to biochemical recurrence after radical prostatectomy. TIMP1 and TIMP2 are controllers of MMPs and the aim of this study is to evaluate the expression levels of MMPs and their regulators using immunohistochemistry in tissue microarray of localized prostate cancer (PC). MATERIALS AND METHODS: Immune-expression of MMP-9, MMP-2, TIMP1, TIMP-2, MMP-14 and IL8, were analyzed by immunohistochemistry in radical prostatectomy specimens of 40 patients with localized PC who underwent surgery between September 1997 and February 2000. Protein expression was considered as categorical variables, negative or positive. The results of the immune-expression were correlated to Gleason score (GS), pathological stage (TNM), pre-operatory PSA serum levels and biochemical recurrence in a mean follow up period of 92.5 months. RESULTS: The loss of TIMP1 immune-expression was related to biochemical recurrence. When TIMP1 was negative, 56.3% patients recurred versus 22.2% of those whose TIMP1 was positive (p=0.042). MMP-9, MMP-2, IL8 and MMP-14 were positive in the majority of PC. TIMP-2 was negative in all cases. CONCLUSION: Negative immune-expression of TIMP1 is correlated with biochemical recurrence in patients with PC possibly by failing to control MMP-9, an important MMP related to cancer progression. |
format | Online Article Text |
id | pubmed-4756933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-47569332016-05-09 Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer dos Reis, Sabrina Thalita Viana, Nayara Izabel Iscaife, Alexandre Pontes, José Dip, Nelson Antunes, Alberto Azoubel Guimarães, Vanessa Ribeiro Santana, Isaque Nahas, William Carlos Srougi, Miguel Leite, Katia Ramos Moreira Int Braz J Urol Original Article INTRODUCTION AND OBJECTIVE: Overexpression of MMPs has been related to biochemical recurrence after radical prostatectomy. TIMP1 and TIMP2 are controllers of MMPs and the aim of this study is to evaluate the expression levels of MMPs and their regulators using immunohistochemistry in tissue microarray of localized prostate cancer (PC). MATERIALS AND METHODS: Immune-expression of MMP-9, MMP-2, TIMP1, TIMP-2, MMP-14 and IL8, were analyzed by immunohistochemistry in radical prostatectomy specimens of 40 patients with localized PC who underwent surgery between September 1997 and February 2000. Protein expression was considered as categorical variables, negative or positive. The results of the immune-expression were correlated to Gleason score (GS), pathological stage (TNM), pre-operatory PSA serum levels and biochemical recurrence in a mean follow up period of 92.5 months. RESULTS: The loss of TIMP1 immune-expression was related to biochemical recurrence. When TIMP1 was negative, 56.3% patients recurred versus 22.2% of those whose TIMP1 was positive (p=0.042). MMP-9, MMP-2, IL8 and MMP-14 were positive in the majority of PC. TIMP-2 was negative in all cases. CONCLUSION: Negative immune-expression of TIMP1 is correlated with biochemical recurrence in patients with PC possibly by failing to control MMP-9, an important MMP related to cancer progression. Sociedade Brasileira de Urologia 2015 /pmc/articles/PMC4756933/ /pubmed/26742965 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0451 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article dos Reis, Sabrina Thalita Viana, Nayara Izabel Iscaife, Alexandre Pontes, José Dip, Nelson Antunes, Alberto Azoubel Guimarães, Vanessa Ribeiro Santana, Isaque Nahas, William Carlos Srougi, Miguel Leite, Katia Ramos Moreira Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title | Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title_full | Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title_fullStr | Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title_full_unstemmed | Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title_short | Loss of TIMP-1 immune expression and tumor recurrence in localized prostate cancer |
title_sort | loss of timp-1 immune expression and tumor recurrence in localized prostate cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756933/ https://www.ncbi.nlm.nih.gov/pubmed/26742965 http://dx.doi.org/10.1590/S1677-5538.IBJU.2014.0451 |
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