Publication:
Association of adiponectin receptor (Adipo-R1/-R2) expression and colorectal cancer

dc.contributor.authorAyyıldız, Talat
dc.contributor.buuauthorDolar, Enver
dc.contributor.buuauthorUğraş, Nesrin
dc.contributor.buuauthorAdım, Şaduman Balaban
dc.contributor.buuauthorYerci, Ömer
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.departmentTıbbi Patoloji Ana Bilim Dalı
dc.contributor.researcheridAAG-9177-2021
dc.contributor.researcheridAAH-2716-2021
dc.contributor.scopusid6602075084
dc.contributor.scopusid55386535600
dc.contributor.scopusid15730076300
dc.contributor.scopusid6603810549
dc.date.accessioned2022-08-18T13:20:57Z
dc.date.available2022-08-18T13:20:57Z
dc.date.issued2014
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.
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.
dc.identifier.endpage9390
dc.identifier.issn1513-7368
dc.identifier.issue21
dc.identifier.pubmed25422229
dc.identifier.scopus2-s2.0-84918509632
dc.identifier.startpage9385
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.identifier.volume15
dc.identifier.wos000351056100052
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherAsian Pacific Organization Cancer Prevention
dc.relation.collaborationYurt içi
dc.relation.journalAsian Pacific Journal of Cancer Prevention
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAdiponectin receptor
dc.subjectAdipo-R1/-R2
dc.subjectColorectal carcinoma
dc.subjectPrognosis
dc.subjectPlasma adiponectin
dc.subjectColon-cancer
dc.subjectSerum adiponectin
dc.subjectInsulin sensitivity
dc.subjectTissue expression
dc.subjectGastric-cancer
dc.subjectRisk
dc.subjectProtein
dc.subjectObesity
dc.subjectHypoadiponectinemia
dc.subjectOncology
dc.subject.emtreeAdiponectin receptor
dc.subject.emtreeAdenocarcinoma
dc.subject.emtreeAged
dc.subject.emtreeCase control study
dc.subject.emtreeColorectal tumor
dc.subject.emtreeDisease free survival
dc.subject.emtreeFactual database
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeGene expression regulation
dc.subject.emtreeGenetics
dc.subject.emtreeHuman
dc.subject.emtreeImmunohistochemistry
dc.subject.emtreeIncidence
dc.subject.emtreeMale
dc.subject.emtreeMiddle aged
dc.subject.emtreeMortality
dc.subject.emtreeNeedle biopsy
dc.subject.emtreePathology
dc.subject.emtreeReference value
dc.subject.emtreeRetrospective study
dc.subject.emtreeRisk assessment
dc.subject.emtreeSurvival
dc.subject.emtreeTime
dc.subject.meshAdenocarcinoma
dc.subject.meshAged
dc.subject.meshBiopsy, needle
dc.subject.meshCase-control studies
dc.subject.meshColorectal neoplasms
dc.subject.meshDatabases, factual
dc.subject.meshDisease-free survival
dc.subject.meshFemale
dc.subject.meshFollow-up studies
dc.subject.meshGene expression regulation, neoplastic
dc.subject.meshHumans
dc.subject.meshImmunohistochemistry
dc.subject.meshIncidence
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshReceptors, adiponectin
dc.subject.meshReference values
dc.subject.meshRetrospective studies
dc.subject.meshRisk assessment
dc.subject.meshSurvival analysis
dc.subject.meshTime factors
dc.subject.scopusLeptin Receptors; Adiponectin; Obesity
dc.subject.wosOncology
dc.titleAssociation of adiponectin receptor (Adipo-R1/-R2) expression and colorectal cancer
dc.typeArticle
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Tıbbi Patoloji Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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