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Correlation Network Analysis Reveals Relationships between MicroRNAs, Transcription Factor T-bet, and Deregulated Cytokine/Chemokine-Receptor Network in Pulmonary Sarcoidosis
T. Dyskova, R. Fillerova, T. Novosad, M. Kudelka, M. Zurkova, P. Gajdos, V. Kolek, E. Kriegova,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT11117
MZ0
CEP - Centrální evidence projektů
NLK
Directory of Open Access Journals
od 1992
Free Medical Journals
od 1992
PubMed Central
od 1992
Europe PubMed Central
od 1992
ProQuest Central
od 2014-01-01
Open Access Digital Library
od 1992-01-01
Open Access Digital Library
od 1992-01-01
Open Access Digital Library
od 1992-01-01
Medline Complete (EBSCOhost)
od 1997-02-01
Health & Medicine (ProQuest)
od 2014-01-01
Wiley-Blackwell Open Access Titles
od 1992
ROAD: Directory of Open Access Scholarly Resources
od 1992
PubMed
26696750
DOI
10.1155/2015/121378
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- genové regulační sítě * MeSH
- lidé středního věku MeSH
- lidé MeSH
- messenger RNA analýza MeSH
- mikro RNA fyziologie MeSH
- plicní sarkoidóza imunologie MeSH
- proteiny T-boxu fyziologie MeSH
- receptory chemokinů genetika MeSH
- receptory cytokinové genetika MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Sarcoidosis is an inflammatory granulomatous disease with unknown etiology driven by cytokines and chemokines. There is limited information regarding the regulation of cytokine/chemokine-receptor network in bronchoalveolar lavage (BAL) cells in pulmonary sarcoidosis, suggesting contribution of miRNAs and transcription factors. We therefore investigated gene expression of 25 inflammation-related miRNAs, 27 cytokines/chemokines/receptors, and a Th1-transcription factor T-bet in unseparated BAL cells obtained from 48 sarcoidosis patients and 14 control subjects using quantitative RT-PCR. We then examined both miRNA-mRNA expressions to enrich relevant relationships. This first study on miRNAs in sarcoid BAL cells detected deregulation of miR-146a, miR-150, miR-202, miR-204, and miR-222 expression comparing to controls. Subanalysis revealed higher number of miR-155, let-7c transcripts in progressing (n = 20) comparing to regressing (n = 28) disease as assessed by 2-year follow-up. Correlation network analysis revealed relationships between microRNAs, transcription factor T-bet, and deregulated cytokine/chemokine-receptor network in sarcoid BAL cells. Furthermore, T-bet showed more pronounced regulatory capability to sarcoidosis-associated cytokines/chemokines/receptors than miRNAs, which may function rather as "fine-tuners" of cytokine/chemokine expression. Our correlation network study implies contribution of both microRNAs and Th1-transcription factor T-bet to the regulation of cytokine/chemokine-receptor network in BAL cells in sarcoidosis. Functional studies are needed to confirm biological relevance of the obtained relationships.
Citace poskytuje Crossref.org
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