Expression of HGF and c-met Detected by Tissue Microarray and Relationship with Tumor Angiogenesis in Human Colorectal Cancer
Ping Ji
Abstract
Ping Ji
Abstract
Objective To study hepatocyte growth factor (HGF) and its receptor (c-met) expressions in human colorectal cancer and non-neoplasm colorectal mucosa,and the relationship with tumor angiogenesis.Methods Tissue microarrays (TMAs) were made up of 80 cases of colorectal cancer and 80 cases of non-neoplasm colorectal mucosa.The expressions of HGF and c-met were detected by immunohistochemistry (SP).CD105 was used as a marker to account microvessel density (MVD) in tumor tissue.Results HGF was over expressed in 48 cases and c-met was over expressed in 63 cases of colorectal cancer tissue,and the correlation between HGF and c-met positive expression was significant (r=0.231,P0.05).The high expression rate of HGF and c-met in colorectal cancer were significantly higher than that in non-neoplasm colorectal mucosa (χ2=35.387,P0.05;χ2=59.854,P0.05) of colorectal cancer.The overexpression of HGF was correlated with lymph node metastasis (χ2=4.743,P0.05) and TNM staging (χ2=5.576,P0.05).The overexpression of c-met was correlated with differentiation (χ2=15.767,P0.05) and lymph node metastasis (χ2=5.765,P0.05) of colorectal cancer.MVD was different between over-expression and low-expression colorectal cancer tissues of HGF and c-met (t=2.150,P0.05;t=2.052,P0.05).There was statistical correlation between HGF and c-met overexpression (r=0.259,P0.05).The overexpressions of HGF and c-met were correlated with lymph metastasis in moderate differentiation cancer (χ2=13.154,P0.05;χ2=5.371,P0.05).Conclusions The overexpressions of HGF and c-met in colorectal cancer may be related with tumor angiogenesis.Detecting the expressions of HGF and c-met is valuable to estimate the biological character of colorectal cancer.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To study hepatocyte growth factor (HGF) and its receptor (c-met) expressions in human colorectal cancer and non-neoplasm colorectal mucosa,and the relationship with tumor angiogenesis.Methods Tissue microarrays (TMAs) were made up of 80 cases of colorectal cancer and 80 cases of non-neoplasm colorectal mucosa.The expressions of HGF and c-met were detected by immunohistochemistry (SP).CD105 was used as a marker to account microvessel density (MVD) in tumor tissue.Results HGF was over expressed in 48 cases and c-met was over expressed in 63 cases of colorectal cancer tissue,and the correlation between HGF and c-met positive expression was significant (r=0.231,P0.05).The high expression rate of HGF and c-met in colorectal cancer were significantly higher than that in non-neoplasm colorectal mucosa (χ2=35.387,P0.05;χ2=59.854,P0.05) of colorectal cancer.The overexpression of HGF was correlated with lymph node metastasis (χ2=4.743,P0.05) and TNM staging (χ2=5.576,P0.05).The overexpression of c-met was correlated with differentiation (χ2=15.767,P0.05) and lymph node metastasis (χ2=5.765,P0.05) of colorectal cancer.MVD was different between over-expression and low-expression colorectal cancer tissues of HGF and c-met (t=2.150,P0.05;t=2.052,P0.05).There was statistical correlation between HGF and c-met overexpression (r=0.259,P0.05).The overexpressions of HGF and c-met were correlated with lymph metastasis in moderate differentiation cancer (χ2=13.154,P0.05;χ2=5.371,P0.05).Conclusions The overexpressions of HGF and c-met in colorectal cancer may be related with tumor angiogenesis.Detecting the expressions of HGF and c-met is valuable to estimate the biological character of colorectal cancer.
Key concepts: Hepatocyte growth factor, Colorectal cancer, Immunohistochemistry, Medicine, Angiogenesis, C-Met, Metastasis, Cancer