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Expression, Epigenetic, and Genetic Changes of HNF1B in Colorectal Lesions: an Analysis of 145 Cases
M. Bártů, J. Hojný, N. Hájková, R. Michálková, E. Krkavcová, K. Simon, V. Frýba, I. Stružinská, K. Němejcová, P. Dundr
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
AZV 17-28404A
Ministerstvo Zdravotnictví Ceské Republiky
RVO64165
Ministerstvo Zdravotnictví Ceské Republiky
Progress Q28/LF1
Univerzita Karlova v Praze
SVV 260367
Univerzita Karlova v Praze (CZ)
CZ.02.1.01/0.0/0.0/18_046/0015959
European Regional Development Fund
BBMRI_CZ LM2018125
European Regional Development Fund
OPPK CZ.2.16/3.1.00/24509
European Regional Development Fund
NV17-28404A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
Medline Complete (EBSCOhost)
od 2014-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1995
- MeSH
- epigeneze genetická * MeSH
- hepatocytární jaderný faktor 1-beta genetika MeSH
- kolorektální nádory genetika metabolismus patologie MeSH
- lidé MeSH
- lokální recidiva nádoru genetika metabolismus patologie MeSH
- metylace DNA * MeSH
- míra přežití MeSH
- nádorové biomarkery genetika MeSH
- následné studie MeSH
- prognóza MeSH
- promotorové oblasti (genetika) MeSH
- regulace genové exprese u nádorů * MeSH
- senioři MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
Hepatocyte nuclear factor 1 beta (HNF1B) is transcription factor which plays a crucial role in the regulation of the development of several organs, but also seems to be implicated in the development of certain tumours, especially the subset of clear cell carcinomas of the ovary and kidney. Depending on the type of the tumour, HNF1B may act as either a tumour suppressor or an oncogene, although the exact mechanism by which HNF1B participates in the process of cancerogenesis is unknown. Using immunohistochemical approach and methylation and mutation analysis, we have investigated the expression, epigenetic, and genetic changes of HNF1B on 40 cases of colorectal adenomas and 105 cases of colorectal carcinomas. The expression of HNF1B was correlated with the benign or malignant behaviour of the lesion, given that carcinomas showed significantly lower levels of expression compared to adenomas. In carcinomas, lower levels of HNF1B expression were associated with recurrence and shortened disease-free survival. The mutation analysis revealed three somatic mutations (two frameshift and one nonsense) in the carcinoma sample set. Promoter methylation was detected in three carcinomas. These results suggest that in colorectal cancer, HNF1B may play a part in the pathogenesis and act in a tumour suppressive fashion.
Citace poskytuje Crossref.org
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