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EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA
BACKGROUND: Gallbladder carcinoma presents a dismal prognosis. Choice treatment is surgical resection that is associated a high levels of both morbidity and mortality. Best knowledgement of prognostic factors may result a better selection of patients either for surgical or multimodal treatment. AIM:...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Colégio Brasileiro de Cirurgia Digestiva
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678687/ https://www.ncbi.nlm.nih.gov/pubmed/25004291 http://dx.doi.org/10.1590/S0102-67202014000200009 |
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author | PAIS-COSTA, Sergio Renato FARAH, José Francisco de Matos ARTIGIANI-NETO, Ricardo MARTINS, Sandro José GOLDENBERG, Alberto |
author_facet | PAIS-COSTA, Sergio Renato FARAH, José Francisco de Matos ARTIGIANI-NETO, Ricardo MARTINS, Sandro José GOLDENBERG, Alberto |
author_sort | PAIS-COSTA, Sergio Renato |
collection | PubMed |
description | BACKGROUND: Gallbladder carcinoma presents a dismal prognosis. Choice treatment is surgical resection that is associated a high levels of both morbidity and mortality. Best knowledgement of prognostic factors may result a better selection of patients either for surgical or multimodal treatment. AIM: To evaluate tecidual immunoexpression of P53, E-cadherin, Cox-2, and EGFR proteins and to correlate these findings with resected gallbladder adenocarcinoma survival. METHODS: Clinical, laboratorial, surgical, and anatomopathological reports of a series of gallbladder adenocarcinoma patients were collected by individualized questionary. Total sample was 42 patients. Median of age was 72 years (35-87). There were seven men and 35 women. Lesion distribuition in according TNM state was the following: T1 (n=2), T2 (n=5), T3 (n=31), T4 (n=4). Twenty-three patients underwent radical resection (R0), while 19 palliative surgery (R1-R2). A block of tissue microarray with neoplasic tissue of each patient was confected. It was performed evaluation of P53, E-Caderine, COX-2, and EGFR proteins imunoexpression. These findings were correlated with overall survival. RESULTS: Five-year survival was 28%. The median of global survival was eight months. Only immunoexpression of EGFR protein was considered independent variable at multivariated analysis. CONCLUSION: Final prognosis was influenced by over-expression of EGFR protein in tumoral tissue. |
format | Online Article Text |
id | pubmed-4678687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Colégio Brasileiro de Cirurgia Digestiva |
record_format | MEDLINE/PubMed |
spelling | pubmed-46786872016-02-24 EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA PAIS-COSTA, Sergio Renato FARAH, José Francisco de Matos ARTIGIANI-NETO, Ricardo MARTINS, Sandro José GOLDENBERG, Alberto Arq Bras Cir Dig Original Article BACKGROUND: Gallbladder carcinoma presents a dismal prognosis. Choice treatment is surgical resection that is associated a high levels of both morbidity and mortality. Best knowledgement of prognostic factors may result a better selection of patients either for surgical or multimodal treatment. AIM: To evaluate tecidual immunoexpression of P53, E-cadherin, Cox-2, and EGFR proteins and to correlate these findings with resected gallbladder adenocarcinoma survival. METHODS: Clinical, laboratorial, surgical, and anatomopathological reports of a series of gallbladder adenocarcinoma patients were collected by individualized questionary. Total sample was 42 patients. Median of age was 72 years (35-87). There were seven men and 35 women. Lesion distribuition in according TNM state was the following: T1 (n=2), T2 (n=5), T3 (n=31), T4 (n=4). Twenty-three patients underwent radical resection (R0), while 19 palliative surgery (R1-R2). A block of tissue microarray with neoplasic tissue of each patient was confected. It was performed evaluation of P53, E-Caderine, COX-2, and EGFR proteins imunoexpression. These findings were correlated with overall survival. RESULTS: Five-year survival was 28%. The median of global survival was eight months. Only immunoexpression of EGFR protein was considered independent variable at multivariated analysis. CONCLUSION: Final prognosis was influenced by over-expression of EGFR protein in tumoral tissue. Colégio Brasileiro de Cirurgia Digestiva 2014 /pmc/articles/PMC4678687/ /pubmed/25004291 http://dx.doi.org/10.1590/S0102-67202014000200009 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article PAIS-COSTA, Sergio Renato FARAH, José Francisco de Matos ARTIGIANI-NETO, Ricardo MARTINS, Sandro José GOLDENBERG, Alberto EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title | EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION
ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title_full | EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION
ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title_fullStr | EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION
ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title_full_unstemmed | EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION
ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title_short | EVALUATION OF P53, E-CADHERIN, COX-2, AND EGFR PROTEIN IMUNNOEXPRESSION
ON PROGNOSTIC OF RESECTED GALLBLADDER CARCINOMA |
title_sort | evaluation of p53, e-cadherin, cox-2, and egfr protein imunnoexpression
on prognostic of resected gallbladder carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678687/ https://www.ncbi.nlm.nih.gov/pubmed/25004291 http://dx.doi.org/10.1590/S0102-67202014000200009 |
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