• Je něco špatně v tomto záznamu ?

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,

. 2015 ; 2015 (-) : 121378. [pub] 20151130

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16027809

Grantová podpora
NT11117 MZ0 CEP - Centrální evidence projektů

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

000      
00000naa a2200000 a 4500
001      
bmc16027809
003      
CZ-PrNML
005      
20190606102847.0
007      
ta
008      
161005s2015 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1155/2015/121378 $2 doi
024    7_
$a 10.1155/2015/121378 $2 doi
035    __
$a (PubMed)26696750
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Tománková, Tereza $u Department of Immunology, Faculty of Medicine and Dentistry, Palacký University, 77515 Olomouc, Czech Republic. $7 xx0199224
245    10
$a Correlation Network Analysis Reveals Relationships between MicroRNAs, Transcription Factor T-bet, and Deregulated Cytokine/Chemokine-Receptor Network in Pulmonary Sarcoidosis / $c T. Dyskova, R. Fillerova, T. Novosad, M. Kudelka, M. Zurkova, P. Gajdos, V. Kolek, E. Kriegova,
520    9_
$a 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.
650    _2
$a dospělí $7 D000328
650    _2
$a senioři $7 D000368
650    _2
$a ženské pohlaví $7 D005260
650    12
$a genové regulační sítě $7 D053263
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a mikro RNA $x fyziologie $7 D035683
650    _2
$a lidé středního věku $7 D008875
650    _2
$a messenger RNA $x analýza $7 D012333
650    _2
$a receptory chemokinů $x genetika $7 D019707
650    _2
$a receptory cytokinové $x genetika $7 D018121
650    _2
$a plicní sarkoidóza $x imunologie $7 D017565
650    _2
$a proteiny T-boxu $x fyziologie $7 D020825
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Fillerová, Regina $u Department of Immunology, Faculty of Medicine and Dentistry, Palacký University, 77515 Olomouc, Czech Republic. $7 xx0147662
700    1_
$a Novosad, Tomas $u IT4Innovations National Supercomputing Center and Faculty of Electrical Engineering and Computer Science, Department of Computer Science, VŠB-Technical University of Ostrava, 70800 Ostrava, Czech Republic.
700    1_
$a Kudelka, Milos $u IT4Innovations National Supercomputing Center and Faculty of Electrical Engineering and Computer Science, Department of Computer Science, VŠB-Technical University of Ostrava, 70800 Ostrava, Czech Republic.
700    1_
$a Žurková, Monika $u Department of Respiratory Diseases, Faculty of Medicine and Dentistry, Palacký University and Faculty Hospital, 77900 Olomouc, Czech Republic. $7 xx0209422
700    1_
$a Gajdos, Petr $u IT4Innovations National Supercomputing Center and Faculty of Electrical Engineering and Computer Science, Department of Computer Science, VŠB-Technical University of Ostrava, 70800 Ostrava, Czech Republic.
700    1_
$a Kolek, Vítězslav, $u Department of Respiratory Diseases, Faculty of Medicine and Dentistry, Palacký University and Faculty Hospital, 77900 Olomouc, Czech Republic. $d 1953-2020 $7 jn20000401390
700    1_
$a Kriegová, Eva, $u Department of Immunology, Faculty of Medicine and Dentistry, Palacký University, 77515 Olomouc, Czech Republic. $d 1968- $7 xx0142572
773    0_
$w MED00006378 $t Mediators of inflammation $x 1466-1861 $g Roč. 2015, č. - (2015), s. 121378
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26696750 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20190606103024 $b ABA008
999    __
$a ok $b bmc $g 1166123 $s 952439
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 2015 $c - $d 121378 $e 20151130 $i 1466-1861 $m Mediators of inflammation $n Mediators Inflamm $x MED00006378
GRA    __
$a NT11117 $p MZ0
LZP    __
$a Pubmed-20161005

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...