Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28260
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dc.contributor.authorAyyıldız, Talat-
dc.date.accessioned2022-08-18T13:20:57Z-
dc.date.available2022-08-18T13:20:57Z-
dc.date.issued2014-
dc.identifier.citationAyyıldız, T. vd. (2014). "Association of adiponectin receptor (Adipo-R1/-R2) expression and colorectal cancer". Asian Pacific Journal of Cancer Prevention, 15(21), 9385-9390.en_US
dc.identifier.issn1513-7368-
dc.identifier.urihttps://doi.org/10.7314/APJCP.2014.15.21.9385-
dc.identifier.urihttp://journal.waocp.org/?sid=Entrez:PubMed&id=pmid:25422229&key=2014.15.21.9385-
dc.identifier.urihttp://hdl.handle.net/11452/28260-
dc.description.abstractIntroduction: Human adiponectin (ApN) is a 30 kDa glycoprotein of 244-amino acids which is extensively produced by adipocytes. ApN acts via two receptors, namely adiponectin receptor-1 (Adipo-R1) and adiponectin receptor-2 (Adipo-R2). Studies have shown the presence of Adipo-R1 and Adipo-R2 expression immunohistochemically in human colorectal cancers (CRCs). However, only a few studies exist which investigated effects of adiponectin receptor expression on CRC characteristics. Objectives: In the present study, we aimed to explore Adipo-R1/-R2 expression in human colorectal cancers and any association with clinicopathological characteristics and survival. Materials and Methods: The study enrolled 58 colorectal cancer patients with tumor resection and a control group of 30 subjects with normal colon mucosa. Results: Positivity for Adipo-R1/-R2 expression was significantly more common in the control group in comparison to the patient group (both p<0.001). There was no significant association between Adipo-R1/-R2 expression and clinicopathological characteristics including age, sex tumor location, pTNM stage, Duke's stage, metastasis, histological differentiation, perineural invasion, venous invasion sex, lymphatic invasion, cancer-related mortality, tumor size and recurrence. AdipoR1/-R2 positivity was also not significantly linked to progression-free or overall survival [p values (0.871, 0.758) and (0.274, 0.232), respectively]. Conclusions: Although significantly reduced Adipo-R1/-R2 expression was found in colorectal cancer patients, it had no influence on survival.en_US
dc.language.isoenen_US
dc.publisherAsian Pacific Organization Cancer Preventionen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAdiponectin receptoren_US
dc.subjectAdipo-R1/-R2en_US
dc.subjectColorectal carcinomaen_US
dc.subjectPrognosisen_US
dc.subjectPlasma adiponectinen_US
dc.subjectColon-canceren_US
dc.subjectSerum adiponectinen_US
dc.subjectInsulin sensitivityen_US
dc.subjectTissue expressionen_US
dc.subjectGastric-canceren_US
dc.subjectRisken_US
dc.subjectProteinen_US
dc.subjectObesityen_US
dc.subjectHypoadiponectinemiaen_US
dc.subjectOncologyen_US
dc.subject.meshAdenocarcinomaen_US
dc.subject.meshAgeden_US
dc.subject.meshBiopsy, needleen_US
dc.subject.meshCase-control studiesen_US
dc.subject.meshColorectal neoplasmsen_US
dc.subject.meshDatabases, factualen_US
dc.subject.meshDisease-free survivalen_US
dc.subject.meshFemaleen_US
dc.subject.meshFollow-up studiesen_US
dc.subject.meshGene expression regulation, neoplasticen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunohistochemistryen_US
dc.subject.meshIncidenceen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshReceptors, adiponectinen_US
dc.subject.meshReference valuesen_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshRisk assessmenten_US
dc.subject.meshSurvival analysisen_US
dc.subject.meshTime factorsen_US
dc.titleAssociation of adiponectin receptor (Adipo-R1/-R2) expression and colorectal canceren_US
dc.typeArticleen_US
dc.identifier.wos000351056100052tr_TR
dc.identifier.scopus2-s2.0-84918509632tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Patoloji Anabilim Dalı.tr_TR
dc.identifier.startpage9385tr_TR
dc.identifier.endpage9390tr_TR
dc.identifier.volume15tr_TR
dc.identifier.issue21tr_TR
dc.relation.journalAsian Pacific Journal of Cancer Preventionen_US
dc.contributor.buuauthorDolar, Enver-
dc.contributor.buuauthorUğraş, Nesrin-
dc.contributor.buuauthorAdım, Şaduman Balaban-
dc.contributor.buuauthorYerci, Ömer-
dc.contributor.researcheridAAG-9177-2021tr_TR
dc.contributor.researcheridAAH-2716-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed25422229tr_TR
dc.subject.wosOncologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid6602075084tr_TR
dc.contributor.scopusid55386535600tr_TR
dc.contributor.scopusid15730076300tr_TR
dc.contributor.scopusid6603810549tr_TR
dc.subject.scopusLeptin Receptors; Adiponectin; Obesityen_US
dc.subject.emtreeAdiponectin receptoren_US
dc.subject.emtreeAdenocarcinomaen_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeCase control studyen_US
dc.subject.emtreeColorectal tumoren_US
dc.subject.emtreeDisease free survivalen_US
dc.subject.emtreeFactual databaseen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeGene expression regulationen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeIncidenceen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeMortalityen_US
dc.subject.emtreeNeedle biopsyen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreeReference valueen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeRisk assessmenten_US
dc.subject.emtreeSurvivalen_US
dc.subject.emtreeTimeen_US
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