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Wilms tumor protein 1 (WT1)-- not only a diagnostic but also a prognostic marker in high-grade serous ovarian carcinoma.
Taube, Eliane Tabea; Denkert, Carsten; Sehouli, Jalid; Kunze, Catarina Alisa; Dietel, Manfred; Braicu, Ioana; Letsch, Anne; Darb-Esfahani, Silvia.
Afiliação
  • Taube ET; Institute of Pathology, Charité University Hospital, Berlin, Germany. Electronic address: eliane.taube@charite.de.
  • Denkert C; Institute of Pathology, Charité University Hospital, Berlin, Germany; Tumor Bank Ovarian Cancer Network (TOC), Berlin, Germany.
  • Sehouli J; Tumor Bank Ovarian Cancer Network (TOC), Berlin, Germany; Department of Gynecology, Charité University Hospital, Berlin, Germany.
  • Kunze CA; Institute of Pathology, Charité University Hospital, Berlin, Germany.
  • Dietel M; Institute of Pathology, Charité University Hospital, Berlin, Germany.
  • Braicu I; Tumor Bank Ovarian Cancer Network (TOC), Berlin, Germany; Department of Gynecology, Charité University Hospital, Berlin, Germany.
  • Letsch A; Department of Hematology and Oncology, Charité University Hospital, Berlin, Germany.
  • Darb-Esfahani S; Institute of Pathology, Charité University Hospital, Berlin, Germany; Tumor Bank Ovarian Cancer Network (TOC), Berlin, Germany.
Gynecol Oncol ; 140(3): 494-502, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26721227
AIMS: Wilms tumor protein 1 (WT1) expression is used in gynecological pathology as a diagnostic marker of serous differentiation, and is frequently co-expressed with ER-α. Early phase studies on WT1 vaccine in gynecological cancers are ongoing. In this study we aimed to determine the prognostic value of WT1 in high-grade serous ovarian carcinoma. METHODS: WT1 protein expression was determined by immunohistochemistry in a cohort of 207 primary high-grade serous ovarian carcinomas. WT1 mRNA expression was evaluated in a cohort of 1137 ovarian carcinomas from publically available gene expression datasets. RESULTS: High WT1 expression was a significant positive prognostic factor in primary high-grade serous ovarian carcinoma regarding overall survival (OS, p=0.008) and progression free survival (PFS, p=0.015), which was independent of age, stage, and residual tumor (OS: p=0.024, PFS: p=0.047). The prognostic significance of immunohistochemical WT1 expression could be reproduced in an independent cohort of 72 patients. On the mRNA level the prognostic significance was validated in silico in publically available gene expression datasets including TCGA data (OS: p=0.002, PFS: p=0.011). WT1 expression was significantly linked to ER-α expression (p=0.001), and tumors that co-expressed both markers (WT1+/ER-α+) had a longer survival time than tumors of all other marker combinations (OS: p=0.002, PFS: p=0.013). CONCLUSION: We present WT1 as a robust prognostic marker in high-grade serous ovarian carcinoma, which adds prognostic information to ER-α. This should be kept in mind when WT1 is used as a biomarker in the context of WT1-targeting therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / RNA Mensageiro / Carcinoma / Proteínas WT1 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / RNA Mensageiro / Carcinoma / Proteínas WT1 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article