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Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters

PURPOSE: To analyze gene and protein expression of metalloproteinases 1, 2, 9, 11 and 16 and their correlation with clinicopathological variables in colorectal adenocarcinoma. METHODS: A retrospective study of 114 patients with colorectal adenocarcinoma treated surgically in the period 2006 to 2008...

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Autores principales: Morini, Sandra Regina, Denadai, Marcos Vinicius, Waisberg, Jaques, Lopes, Gaspar de Jesus, Matos, Delcio, Saad, Sarhan Sydney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433662/
https://www.ncbi.nlm.nih.gov/pubmed/32813775
http://dx.doi.org/10.1590/s0102-865020200070000007
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author Morini, Sandra Regina
Denadai, Marcos Vinicius
Waisberg, Jaques
Lopes, Gaspar de Jesus
Matos, Delcio
Saad, Sarhan Sydney
author_facet Morini, Sandra Regina
Denadai, Marcos Vinicius
Waisberg, Jaques
Lopes, Gaspar de Jesus
Matos, Delcio
Saad, Sarhan Sydney
author_sort Morini, Sandra Regina
collection PubMed
description PURPOSE: To analyze gene and protein expression of metalloproteinases 1, 2, 9, 11 and 16 and their correlation with clinicopathological variables in colorectal adenocarcinoma. METHODS: A retrospective study of 114 patients with colorectal adenocarcinoma treated surgically in the period 2006 to 2008 in Hospital de Câncer de Barretos - Fundação Pio XII. The evaluation of gene expression was performed by RT-PCR, and protein by immunohistochemistry. The analysis of gene expression was classified as overexpressed genes and poorly expressed (fold change of approximately 2, p<0.05). The positivity of the markers in the immunohistochemical study was performed by semi-quantitative analysis. The tissue of TMA (Tissue Microarray) was done by two independent pathologists. RESULTS: The gene expression validated by immuno - histochemical was MMP-1(p= 0.00 and 1.57 fold change) and MMP – 2 (p= 0.01 and – 1.84 to fold change) when correlated with the histological types mucinous and adenocarcinoma NOS, MMP9 (p=0.01 and fold change of 1.13) and MMP-16 (p=0.03 and 1.61 fold change) when compared with the histological types villous and adenocarcinoma NOS, MMP - 11 statistically significant in relation to male (p = 0.04 and 1.65 fold change). CONCLUSIONS: The MMPs 1, 2, 9, 11 and 16 gene and protein expression with statistical significance in at least one of the clinicopathological variables studied. Thus, we conclude that these MMPs have potential as a prognostic factor in colorectal adenocarcinoma.
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spelling pubmed-74336622020-08-25 Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters Morini, Sandra Regina Denadai, Marcos Vinicius Waisberg, Jaques Lopes, Gaspar de Jesus Matos, Delcio Saad, Sarhan Sydney Acta Cir Bras Clinical Investigation PURPOSE: To analyze gene and protein expression of metalloproteinases 1, 2, 9, 11 and 16 and their correlation with clinicopathological variables in colorectal adenocarcinoma. METHODS: A retrospective study of 114 patients with colorectal adenocarcinoma treated surgically in the period 2006 to 2008 in Hospital de Câncer de Barretos - Fundação Pio XII. The evaluation of gene expression was performed by RT-PCR, and protein by immunohistochemistry. The analysis of gene expression was classified as overexpressed genes and poorly expressed (fold change of approximately 2, p<0.05). The positivity of the markers in the immunohistochemical study was performed by semi-quantitative analysis. The tissue of TMA (Tissue Microarray) was done by two independent pathologists. RESULTS: The gene expression validated by immuno - histochemical was MMP-1(p= 0.00 and 1.57 fold change) and MMP – 2 (p= 0.01 and – 1.84 to fold change) when correlated with the histological types mucinous and adenocarcinoma NOS, MMP9 (p=0.01 and fold change of 1.13) and MMP-16 (p=0.03 and 1.61 fold change) when compared with the histological types villous and adenocarcinoma NOS, MMP - 11 statistically significant in relation to male (p = 0.04 and 1.65 fold change). CONCLUSIONS: The MMPs 1, 2, 9, 11 and 16 gene and protein expression with statistical significance in at least one of the clinicopathological variables studied. Thus, we conclude that these MMPs have potential as a prognostic factor in colorectal adenocarcinoma. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2020-08-14 /pmc/articles/PMC7433662/ /pubmed/32813775 http://dx.doi.org/10.1590/s0102-865020200070000007 Text en https://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 Clinical Investigation
Morini, Sandra Regina
Denadai, Marcos Vinicius
Waisberg, Jaques
Lopes, Gaspar de Jesus
Matos, Delcio
Saad, Sarhan Sydney
Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title_full Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title_fullStr Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title_full_unstemmed Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title_short Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
title_sort metalloproteinases and colorectal cancer. correlation of gene expression and clinical-pathological parameters
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7433662/
https://www.ncbi.nlm.nih.gov/pubmed/32813775
http://dx.doi.org/10.1590/s0102-865020200070000007
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