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The SOCS-1-1478CA/del polymorphism is not associated with colorectal cancer or age at onset in Turkish subjects

dc.contributor.buuauthorHartavi, Mustafa
dc.contributor.buuauthorKurt, Ender
dc.contributor.buuauthorOral, Haluk Barbaros
dc.contributor.buuauthorÖlmez, Ömer Fatih
dc.contributor.buuauthorÇubukçu, Erdem
dc.contributor.buuauthorDeligönül, Adem
dc.contributor.buuauthorAvcı, Nilüfer
dc.contributor.buuauthorManavoǧlu, Osman
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentDahiliye Ana Bilim Dalı
dc.contributor.departmentİmmünoloji Bölümü
dc.contributor.departmentOnkoloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-0463-6818
dc.contributor.researcheridK-7285-2012
dc.contributor.scopusid55370753300
dc.contributor.scopusid7006207332
dc.contributor.scopusid7004498001
dc.contributor.scopusid26435400000
dc.contributor.scopusid53986153800
dc.contributor.scopusid37088030300
dc.contributor.scopusid55390409800
dc.contributor.scopusid6602587152
dc.date.accessioned2023-06-23T10:10:24Z
dc.date.available2023-06-23T10:10:24Z
dc.date.issued2013
dc.description.abstractBackground: Suppressor of cytokine signaling (SOCS)-1 acts as a key regulator of many cytokine signaling pathways and its abnormal expression has been identified in several human malignancies, suggesting potential roles in carcinogenesis. The aim of this study was to investigate any association between the functional SOCS-1 -1478CA>del polymorphism and colorectal cancer (CC) as well as age at onset in a Turkish clinical sample. Materials and Methods: A total of 122 subjects were enrolled in this case-control study (70 CC cases and 52 controls). The SOCS-1 -1478CA>del polymorphism was genotyped using a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Results: The odds ratio of the del allele for CC relative to the CA allele was not significantly different between the groups (OR=0.71, 95% CI=0.41-1.22, p=0.27). This result did not change after adjustment for age and sex on multivariable regression analysis (OR=0.84, 95% CI=0.59-1.34, p=0.53). When the SOCS-1 -1478CA>del polymorphism was analyzed among CC patients in relation to the age at disease onset, we found no significant differences between subjects with the del/del, CA/del, and CA/CA genotypes. Conclusions: The results of our study did not point towards a major role of the SOCS-1 -1478CA>del polymorphism in the pathogenesis of CC in Turkish subjects.
dc.identifier.citationHartavi, M. vd. (2013). “The SOCS-1-1478CA/del polymorphism is not associated with colorectal cancer or age at onset in Turkish subjects”. Asian Pacific Journal of Cancer Prevention, 14(12), 7583-7586.
dc.identifier.doi10.7314/APJCP.2013.14.12.7583
dc.identifier.endpage7586
dc.identifier.issn1513-7368
dc.identifier.issue12
dc.identifier.pubmed24460337
dc.identifier.scopus2-s2.0-84893384011
dc.identifier.startpage7583
dc.identifier.urihttps://doi.org/10.7314/APJCP.2013.14.12.7583
dc.identifier.urihttp://koreascience.or.kr/article/JAKO201305981342565.page
dc.identifier.urihttp://hdl.handle.net/11452/33144
dc.identifier.volume14
dc.identifier.wos000331528900089
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherAsian Pacific Organization Cancer Prevention
dc.relation.journalAsian Pacific Journal of Cancer Prevention
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectOncology
dc.subjectColorectal cancer
dc.subjectAge at onset
dc.subjectSuppressor of cytokine signaling
dc.subjectPolymorphism
dc.subjectAssociation study
dc.subjectTyrosine kinase
dc.subjectColon-cancer
dc.subjectRisk-factors
dc.subjectIfn-gamma
dc.subjectSuppressor
dc.subjectInflammation
dc.subjectProgression
dc.subjectMethylation
dc.subjectCarcinomas
dc.subjectAdenomas
dc.subject.emtreeSOCS1 protein, human
dc.subject.emtreeSuppressor of cytokine signaling
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeCase control study
dc.subject.emtreeColorectal tumor
dc.subject.emtreeComparative study
dc.subject.emtreeFemale
dc.subject.emtreeFollow up
dc.subject.emtreeGene deletion
dc.subject.emtreeGenetic polymorphism
dc.subject.emtreeGenetic predisposition
dc.subject.emtreeGenetics
dc.subject.emtreeGenotype
dc.subject.emtreeHuman
dc.subject.emtreeMale
dc.subject.emtreeMiddle aged
dc.subject.emtreeOnset age
dc.subject.emtreePolymerase chain reaction
dc.subject.emtreePrognosis
dc.subject.emtreeRestriction fragment length polymorphism
dc.subject.emtreeTurkey (republic)
dc.subject.meshAdult
dc.subject.meshAge of onset
dc.subject.meshCase-control studies
dc.subject.meshColorectal neoplasms
dc.subject.meshFemale
dc.subject.meshFollow-up studies
dc.subject.meshGene deletion
dc.subject.meshGenetic predisposition to disease
dc.subject.meshGenotype
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshPolymerase chain reaction
dc.subject.meshPolymorphism, genetic
dc.subject.meshPolymorphism, restriction fragment length
dc.subject.meshPrognosis
dc.subject.meshSuppressor of cytokine signaling proteins
dc.subject.meshTurkey
dc.subject.scopusSuppressor of Cytokine Signaling; Suppressors; Cytokines
dc.subject.wosOncology
dc.titleThe SOCS-1-1478CA/del polymorphism is not associated with colorectal cancer or age at onset in Turkish subjects
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Dahiliye Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Onkoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/İmmünoloji Bölümü
local.indexed.atPubMed
local.indexed.atWOS

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