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LI Gang, WANG Wan-li, WEI Li. Expression of E-cadherin, β-catenin and FAK in Colorectal Carcinoma and Their Significances[J]. Cancer Research on Prevention and Treatment, 2005, 32(09): 542-544. DOI: 10.3971/j.issn.1000-8578.533
Citation: LI Gang, WANG Wan-li, WEI Li. Expression of E-cadherin, β-catenin and FAK in Colorectal Carcinoma and Their Significances[J]. Cancer Research on Prevention and Treatment, 2005, 32(09): 542-544. DOI: 10.3971/j.issn.1000-8578.533

Expression of E-cadherin, β-catenin and FAK in Colorectal Carcinoma and Their Significances

  • Objective  To investing ate the role of β-catenin, E-cadherin and FAK in the carcinogenesis and rogression of colorectal carcinoma. Methods  Expression of β-catenin, E-cadherin and FAK was examined immunohistochemically in 12 cases of normal colorectal mucosa, 28 cases of colorectal adenoma, 49 cases of colorectal carcinoma. Results  The rate of cytoplasmic and/or nuclear expression of β-catenin was 61. 2 % in coloretal arcinoma, which was significantly higher than that in colorectal adenoma (35. 7 %, P< 0. 05 ) . The rate of the reduced membranous expression of β-catenin and E-cadherin was 67. 3 %, 57. 1 % respectively in colorectal carcinoma, which was significantly higher than that in the colorectal adenoma and normal colorectal epithelium. The rate of FAK expression was 65. 3 % in colorectal carcinoma, which was significantly higher than that in the colorectal adenoma and in the normal colorectal epithelium ( P < 0. 01) . In addition, the last four kinds of expression was associated with degree of soakage, lymph node metastasis and Dukes stage. There was a positive correlation between FA K expression and the reduced membranous expression of β-catenin might play a role in the carcinogenesis and progression of colorectal carcinoma. Conclusion  The cytoplasmic and/ or nuclear expression of β-catenin, the reduced membranous expression of β-catenin and E-cadherin and FAK expression might be related to the invasion and etastasis of colorectal carcinoma, In which FAK might restrain the adhesion among carcinoma cells.
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