Expression, Epigenetic and Genetic Changes of HNF1B in Endometrial Lesions
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26685938
DOI
10.1007/s12253-015-0037-2
PII: 10.1007/s12253-015-0037-2
Knihovny.cz E-zdroje
- Klíčová slova
- Clear cell carcinoma, Endometrioid carcinoma, HNF-1-beta, Immunohistochemistry, Methylation, Mutation analysis,
- MeSH
- adenokarcinom z jasných buněk genetika patologie MeSH
- endometroidní karcinom genetika patologie MeSH
- epigeneze genetická genetika MeSH
- epigenomika metody MeSH
- genetická variace genetika MeSH
- hepatocytární jaderný faktor 1-beta genetika MeSH
- imunohistochemie metody MeSH
- lidé MeSH
- metylace DNA genetika MeSH
- nádorové biomarkery genetika MeSH
- nádory endometria genetika patologie MeSH
- promotorové oblasti (genetika) genetika MeSH
- serózní cystadenokarcinom genetika patologie MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- hepatocytární jaderný faktor 1-beta MeSH
- HNF1B protein, human MeSH Prohlížeč
- nádorové biomarkery MeSH
Hepatocyte nuclear factor 1-beta (HNF-1-beta) is a transcription factor involved in cancerogenesis of various tumors, including endometrioid carcinoma. We performed comprehensive analysis of HNF-1-beta in lesions of the endometrium, including protein expression and genetic and epigenetic changes. Expression of HNF-1-beta was analyzed immunohistochemically in 320 cases including both tumor and non-tumor endometrial lesions. Promoter methylation and genetic variants were evaluated, using bisulphite and direct sequencing, in 30 (18 fresh frozen, 12 FFPE tumors) endometrioid carcinomas (ECs) and 15 ovarian clear cell carcinomas (OCCCs) as a control group. We detected expression of HNF-1-beta in 28 % of ECs (51/180 cases), 26 % of serous carcinoma (7/27 cases), 83 % of endometrial clear cell carcinoma (15/18 cases), 93 % of hyperplastic polyps with atypias (13/14 cases), 100 % of hyperplastic polyps without atypias (16/16 cases), 88 % of hyperplasias with atypias (14/16 cases), 91 % of hyperplasias without atypias (10/11 cases), and in ≥80 % of different normal endometrium samples. The control group of OCCCs showed HNF-1-beta expression in 95 % (18/19 cases). Methylation in promoter region was detected in 13.3 % (4/30) of ECs, but not in corresponding normal tissue where available, nor in OCCCs (0/15 cases). Mutation analysis revealed truncating variant c.454C > T (p.Gln152X) in one EC and missense variant c.848C > T (p.Ala283Val) was detected in one OCCC. In conclusion, expression of HNF-1-beta was detected in various extents in all types of lesions analyzed, nevertheless its strong expression was mostly limited to clear cell carcinomas. Biological significance of genetic and epigenetic changes needs further investigation.
1st Faculty of Medicine Charles University Prague Prague Czech Republic
Bank of Biological Material 1st Faculty of Medicine Charles University Prague Prague Czech Republic
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