2004TumoriRequires access

Relationship between the expression of E-cadherin,matrix metalloproteinase-2 and the invasion and metastasis of colorectal cancer

Yajun Tao

Open publisher page 0 citations

Abstract

Objective To investigate the role of the expression of E-cadherin(E-Cad) and matrix metalloproteinase-2 (MMP-2) in carcinogensis and progression of colorectal cancer(CRC). Methods The E-Cad and MMP-2 expressions were studied immunohistochemically in 30 specimens of colorectal adenoma and 60 specimens of CRC. Results The expression rates of E-Cad were 87.10﹪ in colorectal adenoma and 55.00﹪ in CRC( P 0.05). Significant relationship was observed between low E-Cad expression and cellular dedifferentiation but negative correlation to metastasis of lymph node and distant organs. The expression rate of MMP-2 was 26.67﹪ in colorectal adenoma significantly lower than the 86.67% in CRC( P 0.05). MMP-2 expression was closely related to cancer growth type,Dukes stage,cellular differentiation,and metastasis to lymph node and distant organs. Conclusion The detection of E-Cad and MMP-2 expression may be helpful to judge the malignant behavier,metastasis and prognosis of colorectal carcinoma.

About this research paper

What this paper is about

Objective To investigate the role of the expression of E-cadherin(E-Cad) and matrix metalloproteinase-2 (MMP-2) in carcinogensis and progression of colorectal cancer(CRC). Methods The E-Cad and MMP-2 expressions were studied immunohistochemically in 30 specimens of colorectal adenoma and 60 specimens of CRC. Results The expression rates of E-Cad were 87.10﹪ in colorectal adenoma and 55.00﹪ in CRC( P 0.05). Significant relationship was observed between low E-Cad expression and cellular dedifferentiation but negative correlation to metastasis of lymph node and distant organs. The expression rate of MMP-2 was 26.67﹪ in colorectal adenoma significantly lower than the 86.67% in CRC( P 0.05). MMP-2 expression was closely related to cancer growth type,Dukes stage,cellular differentiation,and metastasis to lymph node and distant organs. Conclusion The detection of E-Cad and MMP-2 expression may be helpful to judge the malignant behavier,metastasis and prognosis of colorectal carcinoma.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the role of the expression of E-cadherin(E-Cad) and matrix metalloproteinase-2 (MMP-2) in carcinogensis and progression of colorectal cancer(CRC). Methods The E-Cad and MMP-2 expressions were studied immunohistochemically in 30 specimens of colorectal adenoma and 60 specimens of CRC. Results The expression rates of E-Cad were 87.10﹪ in colorectal adenoma and 55.00﹪ in CRC( P 0.05). Significant relationship was observed between low E-Cad expression and cellular dedifferentiation but negative correlation to metastasis of lymph node and distant organs. The expression rate of MMP-2 was 26.67﹪ in colorectal adenoma significantly lower than the 86.67% in CRC( P 0.05). MMP-2 expression was closely related to cancer growth type,Dukes stage,cellular differentiation,and metastasis to lymph node and distant organs. Conclusion The detection of E-Cad and MMP-2 expression may be helpful to judge the malignant behavier,metastasis and prognosis of colorectal carcinoma.

Key concepts: Colorectal cancer, Cadherin, Metastasis, Medicine, Matrix metalloproteinase, Lymph node metastasis, Stage (stratigraphy), Adenoma

Related papers

Back to paper searchBrowse research topicsOriginal source
Relationship between the expression of E-cadherin,matrix metalloproteinase-2 and the invasion and metastasis of colorectal cancer — Research Paper | ScholarLens