Scopus:
The effect of CTLA-4 and CD28 gene variants and circulating protein levels in patients with gastric cancer

dc.contributor.authorArikan S.
dc.contributor.authorGümüş A.
dc.contributor.authorKüçükhüseyin Ö.
dc.contributor.authorCoşkun C.
dc.contributor.authorTuran S.
dc.contributor.authorCacina C.
dc.contributor.authorTalu C.K.
dc.contributor.authorAkyüz F.
dc.contributor.authorFarooqi A.A.
dc.contributor.authorKıran B.
dc.contributor.authorYaylım İ.
dc.date.accessioned2023-04-12T02:25:42Z
dc.date.available2023-04-12T02:25:42Z
dc.date.issued2017-10-01
dc.description.abstractObjective: Gastric cancer is one of the most common malignancies worldwide. The risk factors for gastric cancer include environmental and genetic factors. Inflammation and the immune system are known to contribute to the development of the gastric cancer. We examined the influence of critical polymorphisms of CTLA-4 and CD28 genes and circulating protein levels on the etiology of gastric cancer. Methods: Genotyping of SNPs was performed in 55 gastric cancer patients and 105 healthy individuals using the PCR-RFLP method, and circulating levels of sCTLA-4 and sCD28 were measured. Results: There were no significant differences in the genotype and allele distributions of the evaluated SNPs [CTLA- 4-318 C > T (rs5742909), CTLA-4 + 49 A > G (rs231775), CD28 C > T (rs3116496)] between gastric cancer patients and controls (p = 0.36, p = 0.78, and p = 0.80, respectively). The circulating levels of sCTLA-4 and sCD28 were significantly different between the gastric cancer group and the control group (p < 0.001 and p < 0.001, respectively). Conclusion: The present results suggest that the CTLA-4 and CD28 gene polymorphisms that were evaluated do not play an important role in Turkish patients with gastric cancer. However, sCTLA4 and sCD28 levels were higher in cancer patients and may be useful as an auxiliary parameter in the diagnosis and monitoring of gastric cancer.
dc.identifier.doi10.1515/tjb-2017-0024
dc.identifier.issn02504685
dc.identifier.scopus2-s2.0-85037600785
dc.identifier.urihttps://hdl.handle.net/20.500.12597/5476
dc.relation.ispartofTurkish Journal of Biochemistry
dc.rightstrue
dc.subjectCluster of differentiation 28 (CD28) | Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) | Gastric cancer | Polymerase chain reaction (PCR) | Single nucleotide polymorphism (SNPS)
dc.titleThe effect of CTLA-4 and CD28 gene variants and circulating protein levels in patients with gastric cancer
dc.typeArticle
dspace.entity.typeScopus
oaire.citation.issue5
oaire.citation.volume42
person.affiliation.nameHaseki Education and Research Hospital
person.affiliation.nameBiochemistry
person.affiliation.nameİstanbul Tıp Fakültesi
person.affiliation.nameHaseki Training and Research Hospital
person.affiliation.nameİstanbul Tıp Fakültesi
person.affiliation.nameİstanbul Tıp Fakültesi
person.affiliation.nameHaseki Education and Research Hospital
person.affiliation.nameİstanbul Tıp Fakültesi
person.affiliation.nameIstanbul Medical Faculty
person.affiliation.nameKastamonu University
person.affiliation.nameİstanbul Tıp Fakültesi
person.identifier.scopus-author-id55962065600
person.identifier.scopus-author-id24171456100
person.identifier.scopus-author-id28167476100
person.identifier.scopus-author-id16400695900
person.identifier.scopus-author-id55682005200
person.identifier.scopus-author-id35602740700
person.identifier.scopus-author-id57191837247
person.identifier.scopus-author-id6603943887
person.identifier.scopus-author-id36809549500
person.identifier.scopus-author-id7004830306
person.identifier.scopus-author-id6603287153
relation.isPublicationOfScopus7f548b5d-c962-4a38-b2a9-5591a6b3fd8b
relation.isPublicationOfScopus.latestForDiscovery7f548b5d-c962-4a38-b2a9-5591a6b3fd8b

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