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Metalloproteinases and colorectal cancer. Correlation of gene expression and clinical-pathological parameters
Morini, Sandra Regina; Denadai, Marcos Vinicius; Waisberg, Jaques; Lopes Filho, Gaspar de Jesus; Matos, Delcio; Saad, Sarhan Sydney.
Afiliação
  • Morini, Sandra Regina; Fundação Pio XII. Hospital do Câncer de Barretos. Department of Pathological Anatomy. Barretos. Brazil
  • Denadai, Marcos Vinicius; Fundação Pio XII. Hospital do Câncer de Barretos. Department of Pathological Anatomy. Barretos. Brazil
  • Waisberg, Jaques; Universidade Federal de São Paulo. Department of Medicine. Brazil
  • Lopes Filho, Gaspar de Jesus; Faculdade de Medicina do ABC. Department of Surgery. Santo Andre. Brazil
  • Matos, Delcio; Universidade Federal de São Paulo. Department of Surgery. Sao Paulo. Brazil
  • Saad, Sarhan Sydney; Universidade Federal de São Paulo. Department of Surgery. Sao Paulo. Brazil
Acta cir. bras. ; 35(7): e202000707, 2020. tab
Article em En | VETINDEX | ID: vti-27567
Biblioteca responsável: BR68.1
Localização: BR68.1
ABSTRACT

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.(AU)
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