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Clin Cancer Res ; 17(2): 328-36, 2011 Jan 15.
Article in English | MEDLINE | ID: mdl-21088256

ABSTRACT

PURPOSE: Activation of the Wnt/ß-catenin signaling pathway is frequent in adrenocortical carcinoma (ACC) and might be associated with a more aggressive phenotype. The objective of this study was to assess the prognostic value of ß-catenin immunohistochemistry and CTNNB1 (ß-catenin gene)/APC (adenomatous polyposis coli gene) mutations in patients with resected primary ACC. EXPERIMENTAL DESIGN: In 79 patients with resected primary ACC from a French cohort (Cochin-COMETE), ß-catenin expression was assessed on tumor specimens by immunohistochemistry. For patients with available DNA (n = 49), CTNNB1, and APC hotspot (mutation cluster region), were sequenced. Association between these results and the clinicopathologic characteristics of the ACC and overall and disease-free survival were studied. Results were confirmed on a tissue microarray from an independent multicentric cohort of 92 ACC from Germany (German-ENSAT cohort). RESULTS: In the Cochin-COMETE cohort, the presence of a ß-catenin nuclear staining was significantly associated with a higher ENSAT tumor stage (i.e., stages III and IV), higher Weiss score, more frequent necrosis, mitoses, and CTNNB1/APC mutations. ß-Catenin nuclear staining and the presence of CTNNB1/APC mutations were both associated with decreased overall and disease-free survival, and were independent predictive factors of survival in multivariate analysis. The same results were observed in the German-ENSAT cohort. CONCLUSIONS: Wnt/ß-catenin activation, confirmed by the presence of ß-catenin nuclear staining, is an independent prognostic factor of overall and disease-free survival in patients with resected primary ACC.


Subject(s)
Adrenocortical Carcinoma/metabolism , beta Catenin/metabolism , Adrenocortical Carcinoma/genetics , Adrenocortical Carcinoma/mortality , Adult , Disease-Free Survival , Female , Genes, APC , Humans , Immunohistochemistry , Male , Middle Aged , Mutation , Treatment Outcome , beta Catenin/genetics
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