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Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer

PURPOSE: Matrix metalloproteinase-2 (MMP-2) and MMP-7 have been implicated in tumor growth and metastasis. This study aimed to investigate the expressions of MMP-2 and -7 in colorectal cancer and to evaluate their values as prognostic markers. METHODS: Immunohistochemical staining for MMP-2 and -7 w...

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Autores principales: Hong, Seong Woo, Kang, Yun Kyung, Lee, Byungmo, Lee, Woo Yong, Jang, Yeo Gu, Paik, In Wook, Lee, Hyucksang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Coloproctology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145884/
https://www.ncbi.nlm.nih.gov/pubmed/21829768
http://dx.doi.org/10.3393/jksc.2011.27.3.133
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author Hong, Seong Woo
Kang, Yun Kyung
Lee, Byungmo
Lee, Woo Yong
Jang, Yeo Gu
Paik, In Wook
Lee, Hyucksang
author_facet Hong, Seong Woo
Kang, Yun Kyung
Lee, Byungmo
Lee, Woo Yong
Jang, Yeo Gu
Paik, In Wook
Lee, Hyucksang
author_sort Hong, Seong Woo
collection PubMed
description PURPOSE: Matrix metalloproteinase-2 (MMP-2) and MMP-7 have been implicated in tumor growth and metastasis. This study aimed to investigate the expressions of MMP-2 and -7 in colorectal cancer and to evaluate their values as prognostic markers. METHODS: Immunohistochemical staining for MMP-2 and -7 was done in 144 resected colorectal cancer specimens. Clinicopathological data and survival results were compared with regard to the expression results. RESULTS: The expression rates of MMP-2 in tumor cells in the tumor center and the tumor border were 16.7% and 38.9%, respectively. That of MMP-2 in stromal cells was 27.8%. MMP-7 immunoreactivities of tumor cells in the tumor center and the tumor border were 6.9% and 23.6%. The expressions of MMP-2 and MMP-7 were correlated. MMP-2 expression in stromal cells was more increased in the distal part of the colorectum: 8.8% in right colon cancer, 29.5% in left colon cancer and 36.4% in rectal cancer. MMP-2 expression of tumor cells in the tumor border was correlated with T-stage. MMP-7 expression of tumor cells in the tumor border was increased in case of infiltrative cancer compared with fungating tumor. The expression patterns of MMP-2 and -7 were not correlated with other clinicopathological factors, including tumor markers, node metastasis, distant metastasis, lymphatic invasion, tumor differentiation, and recurrence. No significant associations between the overall and disease-free survival rates and the MMP-2 and -7 expression patterns were noted. CONCLUSION: The high expression rates of MMP-2 and -7 in tumor borders suggest that MMP-2 and -7 have some role in tumor invasion, but in this study, MMP-2 and -7 did not appear to be significant predictors of prognosis in colorectal cancer.
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spelling pubmed-31458842011-08-09 Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer Hong, Seong Woo Kang, Yun Kyung Lee, Byungmo Lee, Woo Yong Jang, Yeo Gu Paik, In Wook Lee, Hyucksang J Korean Soc Coloproctol Original Article PURPOSE: Matrix metalloproteinase-2 (MMP-2) and MMP-7 have been implicated in tumor growth and metastasis. This study aimed to investigate the expressions of MMP-2 and -7 in colorectal cancer and to evaluate their values as prognostic markers. METHODS: Immunohistochemical staining for MMP-2 and -7 was done in 144 resected colorectal cancer specimens. Clinicopathological data and survival results were compared with regard to the expression results. RESULTS: The expression rates of MMP-2 in tumor cells in the tumor center and the tumor border were 16.7% and 38.9%, respectively. That of MMP-2 in stromal cells was 27.8%. MMP-7 immunoreactivities of tumor cells in the tumor center and the tumor border were 6.9% and 23.6%. The expressions of MMP-2 and MMP-7 were correlated. MMP-2 expression in stromal cells was more increased in the distal part of the colorectum: 8.8% in right colon cancer, 29.5% in left colon cancer and 36.4% in rectal cancer. MMP-2 expression of tumor cells in the tumor border was correlated with T-stage. MMP-7 expression of tumor cells in the tumor border was increased in case of infiltrative cancer compared with fungating tumor. The expression patterns of MMP-2 and -7 were not correlated with other clinicopathological factors, including tumor markers, node metastasis, distant metastasis, lymphatic invasion, tumor differentiation, and recurrence. No significant associations between the overall and disease-free survival rates and the MMP-2 and -7 expression patterns were noted. CONCLUSION: The high expression rates of MMP-2 and -7 in tumor borders suggest that MMP-2 and -7 have some role in tumor invasion, but in this study, MMP-2 and -7 did not appear to be significant predictors of prognosis in colorectal cancer. The Korean Society of Coloproctology 2011-06 2011-06-30 /pmc/articles/PMC3145884/ /pubmed/21829768 http://dx.doi.org/10.3393/jksc.2011.27.3.133 Text en © 2011 The Korean Society of Coloproctology http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hong, Seong Woo
Kang, Yun Kyung
Lee, Byungmo
Lee, Woo Yong
Jang, Yeo Gu
Paik, In Wook
Lee, Hyucksang
Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title_full Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title_fullStr Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title_full_unstemmed Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title_short Matrix Metalloproteinase-2 and -7 Expression in Colorectal Cancer
title_sort matrix metalloproteinase-2 and -7 expression in colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145884/
https://www.ncbi.nlm.nih.gov/pubmed/21829768
http://dx.doi.org/10.3393/jksc.2011.27.3.133
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