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dc.title | Expression of oxysterol pathway genes in oestrogen-positive breast carcinomas | en |
dc.contributor.author | Kloudová, Alžběta | |
dc.contributor.author | Brynychová, Veronika | |
dc.contributor.author | Václavíková, Radka | |
dc.contributor.author | Vrána, David | |
dc.contributor.author | Gatěk, Jiří | |
dc.contributor.author | Mrhalová, Marcela | |
dc.contributor.author | Kodet, Roman | |
dc.contributor.author | Souček, Pavel | |
dc.relation.ispartof | Clinical Endocrinology | |
dc.identifier.issn | 0300-0664 Scopus Sources, Sherpa/RoMEO, JCR | |
dc.date.issued | 2017 | |
utb.relation.volume | 86 | |
utb.relation.issue | 6 | |
dc.citation.spage | 852 | |
dc.citation.epage | 861 | |
dc.type | article | |
dc.language.iso | en | |
dc.publisher | Blackwell Publishing Ltd. | |
dc.identifier.doi | 10.1111/cen.13337 | |
dc.relation.uri | http://onlinelibrary.wiley.com/doi/10.1111/cen.13337/full | |
dc.subject | breast carcinoma | en |
dc.subject | expression | en |
dc.subject | oestrogen receptor | en |
dc.subject | oxysterols | en |
dc.subject | prognosis | en |
dc.description.abstract | Objective: This study investigated whether gene expression levels of key modulators of the oxysterol signalling pathway modify the prognosis of patients with oestrogen receptor-positive (ER+) breast carcinomas via interaction with endocrine therapy. Context: The prognosis of patients with ER+ breast carcinoma depends on several factors. Previous studies have suggested that some oxygenated forms of cholesterol (oxysterols) bind to oestrogen receptor and anti-oestrogen binding site which may deregulate cholesterol homoeostasis and influence effect of therapy. Design: The expression levels of 70 oxysterol pathway genes were evaluated in a test set of breast carcinomas differing in ER expression. The genes differentially expressed in ER+ tumours were assessed in a comprehensive set of ER+ tumours to evaluate their clinical significance. Patients: A total of 193 primary patients with breast carcinoma were included. Measurements: The transcript levels were determined by quantitative real-time polymerase chain reaction. Results: The expression levels of 23 genes were found to be specifically dysregulated in ER+ tumours compared to ER− tumours of the test set. The expression levels of ABCG2, CYP7B1, CYP24A1, CYP39A1 and CH25H genes were found to be strongly associated with disease stage; however, none of the gene expression levels were associated with disease-free survival in patients treated with endocrine therapy. Conclusions: The expression of a number of oxysterol pathway genes is significantly modulated by ER expression and associated with the clinical stage of patients. However, the expression of oxysterol pathway genes was not found to modify the prognosis of ER+ patients with breast carcinoma treated with endocrine therapy. © 2017 John Wiley & Sons Ltd | en |
utb.faculty | Faculty of Humanities | |
dc.identifier.uri | http://hdl.handle.net/10563/1007355 | |
utb.identifier.obdid | 43876610 | |
utb.identifier.scopus | 2-s2.0-85018900712 | |
utb.identifier.wok | 000403714100013 | |
utb.identifier.pubmed | 28342201 | |
utb.identifier.coden | CLENA | |
utb.source | j-scopus | |
dc.date.accessioned | 2017-09-08T12:14:44Z | |
dc.date.available | 2017-09-08T12:14:44Z | |
dc.description.sponsorship | 15-25618A, MZCR, Ministerstvo Zdravotnictví Ceské Republiky | |
dc.description.sponsorship | Grantova Agentura Ceske Republiky [13-25222J]; Ministry of Health of the Czech Republic [15-25618A]; National Sustainability Program I [LO1503] | |
utb.contributor.internalauthor | Gatěk, Jiří | |
utb.fulltext.affiliation | Alzbeta Kloudova 1,2, Veronika Brynychova 1, Radka Vaclavikova 1, David Vrana 1,3, Jiri Gatek 4,5, Marcela Mrhalova 6, Roman Kodet 6, Pavel Soucek 1,7 1 Toxicogenomics Unit, National Institute of Public Health, Prague, Czech Republic 2 Third Faculty of Medicine, Charles University, Prague, Czech Republic 3 Department of Oncology, Palacky University Medical School and Teaching Hospital, Olomouc, Czech Republic 4 Department of Surgery, Hospital Atlas, Zlin, Czech Republic 5 University of Tomas Bata in Zlin, Zlin, Czech Republic 6 Department of Pathology & Molecular Medicine, Second Faculty of Medicine, Charles University & Motol University Hospital, Prague, Czech Republic 7 Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic Correspondence Pavel Soucek, Toxicogenomics Unit, Department of Toxicology and Safety, National Institute of Public Health, Prague, Czech Republic. Email: pavel.soucek@szu.cz | |
utb.fulltext.dates | Received: 7 October 2016 Revised: 10 February 2017 Accepted: 21 March 2017 |