Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/37123
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dc.contributor.authorÇil, Nazlı-
dc.contributor.authorYaka, Mutlu-
dc.contributor.authorÜnal, Murat Serkant-
dc.contributor.authorDodurga, Yavuz-
dc.contributor.authorTan, Semih-
dc.contributor.authorSeçme, Mücahit-
dc.contributor.authorKaragür, Ege Rıza-
dc.date.accessioned2021-02-02T09:24:06Z
dc.date.available2021-02-02T09:24:06Z
dc.date.issued2020-
dc.identifier.issn0301-4851-
dc.identifier.urihttps://hdl.handle.net/11499/37123-
dc.identifier.urihttps://doi.org/10.1007/s11033-020-05505-4-
dc.description.abstractAsherman syndrome (AS) occurs due to fibrosis or uterine adhesions as a result of damage to the basal layer of the endometrium. The aim of this study is investigating the effects of adipose tissue-derived mesenchymal stem cell (ADMSC) application on the expression of vascular endothelial growth factor (VEGF), insulin-like growth factor (IGF-1), miRNA-98, miRNA199a in endometrial tissue in rats with AS. Study groups were designed as, control (C), Asherman syndrome (AS), AS + oral estrogen (ASO), AS + ADMSC (ASSC), AS + oral estrogen + ADMSC (ASSCO) with 7 samples in each group. Characterization and differentiation experiments were performed in ADMSC obtained. Two weeks after the development of the AS, ADMSC therapy was applied. BrdU (5-bromo-2'-deoxyuridine) labeling was performed to show the presence of ADMSC in the tissues. Rats were sacrificed after 8 weeks and bilateral uterine horn resection was performed. Tissues were fixed in formaldehyde. After routine tissue follow-up, sections were taken and evaluated with hematoxylin eosin staining. VEGF1 and IGF1 expressions were evaluated by immunohistochemical staining and western blot analysis. Expression changes of miR-98 and miR-199a were detected by RT-PCR. Our results showed that stem cells and estrogen giving together reduced inflammation and fibrosis in the endometrium. Immunohistochemistry and western blot results suggested that this effect was achieved especially through IGF-1. In our study, decreased miR-98 and miR-199a expressions were determined in Asherman syndrome. Furthermore, no changes of miRNA expressions were observed in treatment groups. © 2020, Springer Nature B.V.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofMolecular Biology Reportsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAsherman syndromeen_US
dc.subjectIGF-1en_US
dc.subjectMesenchymal stem cellsen_US
dc.subjectmiR-199aen_US
dc.subjectmiR-98en_US
dc.subjectVEGFen_US
dc.subjectbroxuridineen_US
dc.subjecteosinen_US
dc.subjectestrogenen_US
dc.subjectformaldehydeen_US
dc.subjecthematoxylinen_US
dc.subjectmicroRNAen_US
dc.subjectmicroRNA 199aen_US
dc.subjectmicroRNA 98en_US
dc.subjectsomatomedin Cen_US
dc.subjectunclassified drugen_US
dc.subjectvasculotropinen_US
dc.subjectadipose derived stem cellen_US
dc.subjectanimal experimenten_US
dc.subjectanimal modelen_US
dc.subjectanimal tissueen_US
dc.subjectArticleen_US
dc.subjectcontrolled studyen_US
dc.subjectendometriumen_US
dc.subjectfemaleen_US
dc.subjectfibrosisen_US
dc.subjectfollow upen_US
dc.subjectgene expressionen_US
dc.subjectimmunohistochemistryen_US
dc.subjectinflammationen_US
dc.subjectmesenchymal stem cell transplantationen_US
dc.subjectnonhumanen_US
dc.subjectprotein expressionen_US
dc.subjectraten_US
dc.subjectuterus hornen_US
dc.subjectuterus synechiaen_US
dc.subjectWestern blottingen_US
dc.titleAdipose derived mesenchymal stem cell treatment in experimental asherman syndrome induced ratsen_US
dc.typeArticleen_US
dc.identifier.volume47en_US
dc.identifier.issue6en_US
dc.identifier.startpage4541
dc.identifier.startpage4541en_US
dc.identifier.endpage4552en_US
dc.authorid0000-0003-1992-7909-
dc.authorid0000-0002-4936-5954-
dc.authorid0000-0002-5609-9594-
dc.authorid0000-0002-2084-760X-
dc.authorid0000-0001-6794-3685-
dc.identifier.doi10.1007/s11033-020-05505-4-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid32444974en_US
dc.identifier.scopus2-s2.0-85085377537en_US
dc.identifier.wosWOS:000534860700002en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
crisitem.author.dept14.03. Basic Medical Sciences-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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