MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://ar.iiarjournals.org/content/29/11/4807.long http://repositorio.unifesp.br/handle/11600/42594 |
Resumo: | The aim of the present study was to evaluate by immunohistochemistry the prognostic meaning of the tumor marker MET (hepatocyte growth factor) in patients submitted to surgical resection due to primary colorectal adenocarcinoma. Patients and Methods: A retrospective study was carried out that included 286 consecutive patients with colorectal adenocarcinoma, submitted to surgical resection at Barretos Cancer Hospital, from 1993 to 2002. The histopathological expression of the MET tumor marker was evaluated using an anti-protein monoclonal antibody against MET by the streptavidin-biotin-peroxidase technique. The expression of the tumor marker was semi-quantitative, and the slide samples were independently analyzed by three pathologists unaware of patient clinical and histopathological data. Results: The tumor marker expression was positive in 236 (79%) out of a total of 286 patients. This expression was statistically significantly different between stages I and IV (p=0.004), for overall survival (p=0.009), and for cancer-related mortality rates (p=0.022). However, no association between the tumor marker and recurrence (p=0.89) or disease-free interval (p=0.91) was observed. Conclusion: MET has shown significant expression at advanced stages of the disease, as well as for overall survival and cancer-related mortality rates demonstrating to be a valuable marker for poor prognosis in colorectal cancer patients. |
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MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and MortalityColorectal carcinomaimmunohistochemistryMETprognosissurvivalcarcinogenesisThe aim of the present study was to evaluate by immunohistochemistry the prognostic meaning of the tumor marker MET (hepatocyte growth factor) in patients submitted to surgical resection due to primary colorectal adenocarcinoma. Patients and Methods: A retrospective study was carried out that included 286 consecutive patients with colorectal adenocarcinoma, submitted to surgical resection at Barretos Cancer Hospital, from 1993 to 2002. The histopathological expression of the MET tumor marker was evaluated using an anti-protein monoclonal antibody against MET by the streptavidin-biotin-peroxidase technique. The expression of the tumor marker was semi-quantitative, and the slide samples were independently analyzed by three pathologists unaware of patient clinical and histopathological data. Results: The tumor marker expression was positive in 236 (79%) out of a total of 286 patients. This expression was statistically significantly different between stages I and IV (p=0.004), for overall survival (p=0.009), and for cancer-related mortality rates (p=0.022). However, no association between the tumor marker and recurrence (p=0.89) or disease-free interval (p=0.91) was observed. Conclusion: MET has shown significant expression at advanced stages of the disease, as well as for overall survival and cancer-related mortality rates demonstrating to be a valuable marker for poor prognosis in colorectal cancer patients.Barretos Canc Hosp, Pio Fdn 12, Dept Surg, Sao Paulo, BrazilBarretos Canc Hosp, Pio Fdn 12, Dept Pathol, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Gastroenterol, Sch Med, Sao Paulo, BrazilUniv Fed Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, BrazilUniv Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, PortugalUniv Sao Paulo, Sch Med, Dept Pathol, Lab Med Invest LIM 14, Sao Paulo, BrazilUniv Fed Sao Paulo, Dept Gastroenterol, Sch Med, Sao Paulo, BrazilUniv Fed Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, BrazilWeb of ScienceInt Inst Anticancer ResearchBarretos Canc HospUniversidade Federal de São Paulo (UNIFESP)Univ MinhoUniversidade de São Paulo (USP)Oliveira, Antonio Talvane Torres de [UNIFESP]Matos, Delcio [UNIFESP]Logullo, Angela Flavia [UNIFESP]Silva, Sandra Regina Morini da [UNIFESP]Artigiani Neto, Ricardo [UNIFESP]Longat Filho, AdhemarSaad, Sarhan Sydney [UNIFESP]2018-06-15T13:50:15Z2018-06-15T13:50:15Z2009-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion4807-4811http://ar.iiarjournals.org/content/29/11/4807.longAnticancer Research. Athens: Int Inst Anticancer Research, v. 29, n. 11, p. 4807-4811, 2009.0250-7005http://repositorio.unifesp.br/handle/11600/42594WOS:000273203300067engAnticancer Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-05-02T15:52:28Zoai:repositorio.unifesp.br/:11600/42594Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-05-02T15:52:28Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
title |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
spellingShingle |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality Oliveira, Antonio Talvane Torres de [UNIFESP] Colorectal carcinoma immunohistochemistry MET prognosis survival carcinogenesis |
title_short |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
title_full |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
title_fullStr |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
title_full_unstemmed |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
title_sort |
MET Is Highly Expressed in Advanced Stages of Colorectal Cancer and Indicates Worse Prognosis and Mortality |
author |
Oliveira, Antonio Talvane Torres de [UNIFESP] |
author_facet |
Oliveira, Antonio Talvane Torres de [UNIFESP] Matos, Delcio [UNIFESP] Logullo, Angela Flavia [UNIFESP] Silva, Sandra Regina Morini da [UNIFESP] Artigiani Neto, Ricardo [UNIFESP] Longat Filho, Adhemar Saad, Sarhan Sydney [UNIFESP] |
author_role |
author |
author2 |
Matos, Delcio [UNIFESP] Logullo, Angela Flavia [UNIFESP] Silva, Sandra Regina Morini da [UNIFESP] Artigiani Neto, Ricardo [UNIFESP] Longat Filho, Adhemar Saad, Sarhan Sydney [UNIFESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Barretos Canc Hosp Universidade Federal de São Paulo (UNIFESP) Univ Minho Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Oliveira, Antonio Talvane Torres de [UNIFESP] Matos, Delcio [UNIFESP] Logullo, Angela Flavia [UNIFESP] Silva, Sandra Regina Morini da [UNIFESP] Artigiani Neto, Ricardo [UNIFESP] Longat Filho, Adhemar Saad, Sarhan Sydney [UNIFESP] |
dc.subject.por.fl_str_mv |
Colorectal carcinoma immunohistochemistry MET prognosis survival carcinogenesis |
topic |
Colorectal carcinoma immunohistochemistry MET prognosis survival carcinogenesis |
description |
The aim of the present study was to evaluate by immunohistochemistry the prognostic meaning of the tumor marker MET (hepatocyte growth factor) in patients submitted to surgical resection due to primary colorectal adenocarcinoma. Patients and Methods: A retrospective study was carried out that included 286 consecutive patients with colorectal adenocarcinoma, submitted to surgical resection at Barretos Cancer Hospital, from 1993 to 2002. The histopathological expression of the MET tumor marker was evaluated using an anti-protein monoclonal antibody against MET by the streptavidin-biotin-peroxidase technique. The expression of the tumor marker was semi-quantitative, and the slide samples were independently analyzed by three pathologists unaware of patient clinical and histopathological data. Results: The tumor marker expression was positive in 236 (79%) out of a total of 286 patients. This expression was statistically significantly different between stages I and IV (p=0.004), for overall survival (p=0.009), and for cancer-related mortality rates (p=0.022). However, no association between the tumor marker and recurrence (p=0.89) or disease-free interval (p=0.91) was observed. Conclusion: MET has shown significant expression at advanced stages of the disease, as well as for overall survival and cancer-related mortality rates demonstrating to be a valuable marker for poor prognosis in colorectal cancer patients. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-11-01 2018-06-15T13:50:15Z 2018-06-15T13:50:15Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://ar.iiarjournals.org/content/29/11/4807.long Anticancer Research. Athens: Int Inst Anticancer Research, v. 29, n. 11, p. 4807-4811, 2009. 0250-7005 http://repositorio.unifesp.br/handle/11600/42594 WOS:000273203300067 |
url |
http://ar.iiarjournals.org/content/29/11/4807.long http://repositorio.unifesp.br/handle/11600/42594 |
identifier_str_mv |
Anticancer Research. Athens: Int Inst Anticancer Research, v. 29, n. 11, p. 4807-4811, 2009. 0250-7005 WOS:000273203300067 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Anticancer Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
4807-4811 |
dc.publisher.none.fl_str_mv |
Int Inst Anticancer Research |
publisher.none.fl_str_mv |
Int Inst Anticancer Research |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268313783500800 |