Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14365/5368
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dc.contributor.authorBarış, Elif-
dc.contributor.authorDemir, Ayşe Banu-
dc.date.accessioned2024-06-29T13:07:36Z-
dc.date.available2024-06-29T13:07:36Z-
dc.date.issued2024-
dc.identifier.issn0250-4685-
dc.identifier.issn1303-829X-
dc.identifier.urihttps://doi.org/10.1515/tjb-2023-0282-
dc.identifier.urihttps://hdl.handle.net/20.500.14365/5368-
dc.description.abstractObjectives Toll-like receptor (TLR) mediated inflammatory status plays an important role in development and progression of hepatocellular carcinoma (HCC). Toll-interacting protein (TOLLIP) has an inhibitory effect on TLR-mediated inflammatory signalling and expression profile of TOLLIP varies between malignancies including HCC. Cholinergic anti-inflammatory pathway (CAP) is an endogenous mechanism that controls inflammatory status via alpha 7nicotinic acetylcholine receptors (alpha 7nAChR). This study aims to investigate the effect of CAP-acting agent choline on TOLLIP and its related TLR-mediated inflammatory response in HCC cells with distinct differentiation stages.Methods The expression patterns of alpha 7nAChR, TLR2/4, TOLLIP, IL6,NFkB genes were evaluated by RT-PCR and ELISA in the presence of choline, along with the real-time cell proliferation and migration in HEP3B and SNU449 HCC cell lines. The interaction between choline and TOLLIP assessed by using in-silico analyses.Results Choline downregulated TOLLIP in Hep3B and SNU449 cells. However, the expressions of alpha 7nAChR, NF-kappa B, IL-6, TLR2 and TLR4 showed a decreased pattern in well differentiated HEP3B cells, while an increased pattern in poorly differentiated SNU449 cells.Conclusions Choline might exert differential effects in TLR2/4-dependent signalling based on the differentiation stages of the HCC cells, suggesting its potential therapeutic effects in earlier stages of HCC which might be result of its partial modulation of TOLLIP.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [119Z221]en_US
dc.description.sponsorshipThis study was supported by the Scientific and Technological Research Council of Turkey (TUBITAK) (Grant No: 119Z221 given to ABD)en_US
dc.language.isoenen_US
dc.publisherWalter De Gruyter Gmbhen_US
dc.relation.ispartofTurkish Journal of Biochemistry-Turk Biyokimya Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectcholineen_US
dc.subjecthepatocellular carcinomaen_US
dc.subjectinflammationen_US
dc.subjecttoll-like receptoren_US
dc.subjecttoll-interacting proteinen_US
dc.subjectNicotinic Acetylcholine-Receptoren_US
dc.subjectLiver-Canceren_US
dc.subjectInflammationen_US
dc.subjectProliferationen_US
dc.subjectMechanismsen_US
dc.subjectMigrationen_US
dc.subjectInvasionen_US
dc.titleDifferential Effects of Choline on Tlr2/4 Mediated Signaling Through Possible Regulation of Toll-Interacting Protein in Hepatocellular Carcinoma Cell Linesen_US
dc.typeArticleen_US
dc.typeArticle; Early Accessen_US
dc.identifier.doi10.1515/tjb-2023-0282-
dc.identifier.scopus2-s2.0-85202951072en_US
dc.departmentİzmir Ekonomi Üniversitesien_US
dc.authoridBARIS, Elif/0000-0001-6838-7932-
dc.authorwosidBARIS, Elif/HPF-4375-2023-
dc.identifier.wosWOS:001230450000001en_US
dc.institutionauthor-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ4-
dc.identifier.wosqualityQ4-
item.languageiso639-1en-
item.openairetypeArticle-
item.openairetypeArticle; Early Access-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
crisitem.author.dept09.01. Basic Medical Sciences-
crisitem.author.dept09.01. Basic Medical Sciences-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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