Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/46085
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dc.contributor.authorKehrIbar, Demet Yalcin-
dc.contributor.authorOzgen, Metin-
dc.contributor.authorYolbaS, Servet-
dc.contributor.authorYildirim, Ahmet-
dc.contributor.authorTurkmen, Nese Basak-
dc.contributor.authorEtem, Ebru Onalan-
dc.contributor.authorÇiftçi, Osman-
dc.date.accessioned2023-01-09T21:09:25Z-
dc.date.available2023-01-09T21:09:25Z-
dc.date.issued2021-
dc.identifier.issn1300-0144-
dc.identifier.issn1303-6165-
dc.identifier.urihttps://doi.org/10.3906/sag-2008-274-
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/481010-
dc.identifier.urihttps://hdl.handle.net/11499/46085-
dc.description.abstractBackground/aim: The purpose of this study was to investigate the antiarthritic potentials of the inhibition of Src kinase in vivo and in vitro settings. Materials and methods: Arthritis was induced by intradermal injection of chicken type II collagen combined with incomplete Freund's adjuvant (collagen induced arthritis [CIA] model) in Wistar albino rats. One day alter the onset of arthritis, dasatinib, a potent Src kinase inhibitor, (5 mg/kg/day) was given via oral gavage. Tissue Src, Fyn, MAPK and STAT mRNA expressions were determined by real-time polymerase chain reaction. On the other hand, fibroblast like synoviocytes (FLSs) were harvested patients with rheumatoid arthritis (RA) undergoing surgical knee joint replacement. FLSs were stimulated with cytokines and dasatinib was added in different concentrations. MMP -1, -3, and -13 levels in FLSs culture were determined by ELISA. Results: The tissue mRNA expressions of Src, Fyn, MAPK and STATs were increased in the arthritis CIA group compared to the control group. Their mRNA expressions in the CIA + dasatinib group were decreased and similar in the control group. In in vitro setting, MMP -1, -3, and -13 expressions from FLSs induced by IL-1 beta and TNF-alpha were increased, while dasatinib suppressed their productions from FLSs. Conclusion: The present study shows that the inhibition of Src kinase has antiarthritic potentials in both in vivo and in vitro settings. Src kinase inhibition may be candidate to further research in human RA.en_US
dc.description.sponsorship[TF.13.53]en_US
dc.description.sponsorshipThis study supported by Frat universitesi Bilimsel Aratrma Projeleri (TF.13.53) .en_US
dc.language.isoenen_US
dc.publisherTubitak Scientific & Technical Research Council Turkeyen_US
dc.relation.ispartofTurkish Journal Of Medical Sciencesen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectRheumatoid arthritisen_US
dc.subjectcollagen induced arthritisen_US
dc.subjectsrc kinaseen_US
dc.subjectmatrix metalloproteinaseen_US
dc.subjectFamily Kinasesen_US
dc.subjectTnf-Alphaen_US
dc.subjectActivationen_US
dc.subjectExpressionen_US
dc.subjectArthritisen_US
dc.subjectDasatiniben_US
dc.subjectModelen_US
dc.subjectMmp-9en_US
dc.subjectHcken_US
dc.titleThe inhibition of Src kinase suppresses the production of matrix metalloproteinases in from synovial fibroblasts and inhibits MAPK and STATs pathwaysen_US
dc.typeArticleen_US
dc.identifier.volume51en_US
dc.identifier.issue4en_US
dc.identifier.startpage2142en_US
dc.identifier.endpage2149en_US
dc.authoridÖZERCAN, ibrahim Hanifi/0000-0002-8781-8838-
dc.authoridYalcin Kehribar, Demet/0000-0002-1852-7981-
dc.authoridozercan, ibrahim hanifi/0000-0002-2971-3536-
dc.identifier.doi10.3906/sag-2008-274-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid55929839900-
dc.authorscopusid24830886900-
dc.authorscopusid54386385600-
dc.authorscopusid8150282900-
dc.authorscopusid57208011277-
dc.authorscopusid37004699900-
dc.authorscopusid27867577100-
dc.authorwosidÖZERCAN, ibrahim Hanifi/W-7883-2018-
dc.identifier.pmid33714238en_US
dc.identifier.scopus2-s2.0-85106721365en_US
dc.identifier.trdizinid481010en_US
dc.identifier.wosWOS:000691664800007en_US
dc.identifier.scopusqualityQ3-
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.grantfulltextopen-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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