Immunohistochemical expression profile of 尾-catenin, E-cadherin, P-cadherin, laminin-5纬2 chain, and SMAD4 in colorectal serrated adenocarcinoma
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Summary

The immunohistochemical expression of cell adhesion molecules in colorectal serrated adenocarcinoma is still unknown. The immunostaining patterns of -catenin, E-cadherin, P-cadherin, laminin 52, and SMAD4 and their relationship to survival were studied in different tumor areas, namely, tumor center and invasive front, the latter comprising tumor bud and non-tumor bud clusters, as described in a previous study of 66 serrated adenocarcinomas and matched conventional carcinomas. Compared with conventional carcinomas, serrated adenocarcinomas showed significantly reduced nuclear -catenin, membranous E-cadherin, and nuclear SMAD4 but an increased cytoplasmic expression of laminin-52 at the invasive front that was particularly pronounced in the tumor buds. E-cadherin loss at the invasive front was identified as an independent prognostic factor for a poorer outcome in serrated adenocarcinoma. Serrated adenocarcinoma shows a distinct immunohistochemical profile at the invasive front compared with conventional carcinoma, which may account for its less favorable outcome. The lower frequency of nuclear -catenin in SAC, especially in right-sided tumors, suggests that molecular mechanisms other than the canonical Wnt/-catenin pathway may have a role in tumor bud formation.

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