Reduced expression of α catenin is associated with poor prognosis in colorectal carcinoma

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Abstract

Aims - To investigate a catenin expression in surgically resected human colorectal cancers to evaluate its prognostic value during long term follow up. Methods - Immunohistochemistry was used to compare the expression of a catenin with conventional prognostic factors in 187 colorectal cancer patients treated in Kuopio University Hospital and followed up for a mean of 14 years. The hypothesis that the intensity of expression of α catenin and its distribution in cancer cells is correlated with survival was tested with the log-rank test, hazard ratios, and their confidence intervals. Results - Uniform membranous α catenin staining localised to the intercellular borders was observed in 46% of the tumours; 55% of all turnouts had either heterogeneous or negative α catenin expression, and staining intensity was either negative or weak in 42% of the tumours. The cancer related and recurrence-free survival rates were lower among patients with a weak a catenin intensity in turnout epithelium (p < 0.001), a low fraction of positive tumour cells (p < 0.001), and an additional cytoplasmic accumulation of α catenin (p < 0.001). In multivariate analysis, the intensity of α catenin expression in turnout epithelium predicted cancer related survival independently; α catenin localisation in tumour epithelium was an independent prognostic factor of recurrence-free survival in the group as a whole and in the T1-3N0M0 tumour subgroup. Conclusions - A low proportion of positive carcinoma cells, additional cytoplasmic accumulation of α catenin, and reduced expression intensity in tumour epithelium predict a poor survival rate. The results suggest that α catenin has prognostic significance in colorectal cancer.

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Ropponen, K. M., Eskelinen, M. J., Lipponen, P. K., Alhava, E. M., & Kosma, V. M. (1999). Reduced expression of α catenin is associated with poor prognosis in colorectal carcinoma. Journal of Clinical Pathology, 52(1), 10–16. https://doi.org/10.1136/jcp.52.1.10

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