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HNF1B, EZH2 and ECI2 in prostate carcinoma. Molecular, immunohistochemical and clinico-pathological study
P. Dundr, M. Bártů, J. Hojný, R. Michálková, N. Hájková, I. Stružinská, E. Krkavcová, L. Hadravský, L. Kleissnerová, J. Kopejsková, BQ. Hiep, K. Němejcová, R. Jakša, O. Čapoun, J. Řezáč, K. Jirsová, V. Franková
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NV17-28404A
MZ0
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Digital library NLK
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- MeSH
- Dodecenoyl-CoA Isomerase genetics metabolism MeSH
- Enhancer of Zeste Homolog 2 Protein genetics metabolism MeSH
- Hepatocyte Nuclear Factor 1-beta genetics metabolism MeSH
- Prostatic Hyperplasia genetics metabolism pathology MeSH
- Immunohistochemistry methods MeSH
- Cohort Studies MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- DNA Methylation MeSH
- Mutation MeSH
- Prostatic Neoplasms genetics metabolism pathology MeSH
- Prognosis MeSH
- Promoter Regions, Genetic MeSH
- Prostate pathology MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Aged MeSH
- Neoplasm Grading MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Hepatocyte nuclear factor 1 beta (HNF1B) is a tissue specific transcription factor, which seems to play an important role in the carcinogenesis of several tumors. In our study we focused on analyzing HNF1B in prostate carcinoma (PC) and adenomyomatous hyperplasia (AH), as well as its possible relation to the upstream gene EZH2 and downstream gene ECI2. The results of our study showed that on an immunohistochemical level, the expression of HNF1B was low in PC, did not differ between PC and AH, and did not correlate with any clinical outcomes. In PC, mutations of HNF1B gene were rare, but the methylation of its promotor was a common finding and was positively correlated with Gleason score and stage. The relationship between HNF1B and EZH2/ECI2 was equivocal, but EZH2 and ECI2 were positively correlated on both mRNA and protein level. The expression of EZH2 was associated with poor prognosis. ECI2 did not correlate with any clinical outcomes. Our results support the oncosuppressive role of HNF1B in PC, which may be silenced by promotor methylation and other mechanisms, but not by gene mutation. The high expression of EZH2 (especially) and ECI2 in PC seems to be a potential therapeutic target.
References provided by Crossref.org
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