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Expressions of Poly(ADP-ribose) Glycohydrolase(PARG) and Membrane Type 1 Matrix Metalloproteinase(MT1-MMP) in Colorectal Carcinoma 被引量:1
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作者 Xian li Guang-jie Duan +2 位作者 Ya-lan Wang N. Jasmine Fauzee qiao-zhuan li 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2010年第3期186-193,共8页
Objective:To investigate the significance of Poly(ADP-ribose) glycolhydrolase(PARG) and membrane type 1 matrix metalloproteinase(MT1-MMP) expressions in human colorectal carcinoma.Methods:Immunohistochemical s... Objective:To investigate the significance of Poly(ADP-ribose) glycolhydrolase(PARG) and membrane type 1 matrix metalloproteinase(MT1-MMP) expressions in human colorectal carcinoma.Methods:Immunohistochemical staining for PARG and MT1-MMP was carried out on colorectal adenoma-carcinoma tissue microarrays containing normal colorectal mucosae,adenoma,adenoma with malignant transformation and adenocarcinoma(total 130 specimens).The expressions of PARG and MT1-MMP in the GLTN [Gallotannin]-treated and GLTN-untreated lovo cells were detected by Western Blot.Results:PARG expression in adenocarcinoma(83.1%) and adenoma with malignant transformation(66.7%) was significantly higher than that in normal colorectal mucosa(10%) and adenoma(10.5%).Expression of MT1-MMp in normal colorectal mucosa and adenoma was negative,while the expression in adenocarcinoma(80.3%) and adenoma with malignant transformation(72.2%) was high.The expressions of PARG and MT1-MMP in adenocarcinoma with metastasis and in late tumor stages were significantly higher than those in adenocarcinoma with no metastasis and in early tumor stages.Thus,PARG expression shows a positive correlation with the expression of MT1-MMP.The expressions of PARG and MT1-MMP in GLTN-treated lovo cells were weaker than that in GLTN-untreated lovo cells.Conclusion:The expression of PARG was probably related to the development of colorectal carcinoma.PARG may play an important role for the regulation of MT1-MMP expression in colorectal carcinoma. 展开更多
关键词 PARG MT1-MMP Colorectal carcinoma Tissue microarray IMMUNOHISTOCHEMISTRY
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