Logotipo do repositório

Influence of functional polymorphisms in TNF-α, IL-8, and IL-10 cytokine genes on mRNA expression levels and risk of gastric cancer

dc.contributor.authorOliveira, Juliana Garcia de [UNESP]
dc.contributor.authorRossi, Ana Flávia Teixeira [UNESP]
dc.contributor.authorNizato, Daniela Manchini
dc.contributor.authorCadamuro, Aline Cristina Targa [UNESP]
dc.contributor.authorJorge, Yvana Cristina [UNESP]
dc.contributor.authorValsechi, Marina Curado [UNESP]
dc.contributor.authorVenâncio, Larissa Paola Rodrigues [UNESP]
dc.contributor.authorRahal, Paula [UNESP]
dc.contributor.authorPavarino, Érika Cristina
dc.contributor.authorGoloni-Bertollo, Eny Maria
dc.contributor.authorSilva, Ana Elizabete [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade do Sagrado Coração (USC)
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto (FAMERP)
dc.date.accessioned2015-12-07T15:33:21Z
dc.date.available2015-12-07T15:33:21Z
dc.date.issued2015
dc.description.abstractFunctional polymorphisms in promoter regions can produce changes in the affinity of transcription factors, thus altering the messenger ribonucleic acid (mRNA) expression levels of inflammatory cytokines associated with the risk of cancer development. The goal of this study was to evaluate the influence that polymorphisms in the cytokine genes known as TNF-α-308 G/A (rs1800629), TNF-α-857 C/T (rs1799724), IL-8-251 T/A (rs4073), IL-8-845 T/C (rs2227532), and IL-10-592 C/A (rs1800872) have on changes to mRNA expression levels and on the risks of chronic gastritis (CG) and gastric cancer (GC). A sample of 723 individuals was genotyped using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. Relative mRNA expression levels were measured using quantitative real-time PCR (qPCR). Polymorphisms TNF-α-308 G/A and IL-8-251 A/T were not associated with risks of these gastric lesions. However, TNF-α-857 C/T, IL-8-845 T/C, and IL-10-592 C/A were found to be associated with a higher risk of GC, and IL-10-592 C/A was found to be associated with a higher risk of CG. The relative mRNA expression levels (RQ) of TNF-α, IL-8, and IL-10 were markedly downregulated in the CG group (median RQs = 0.128, 0.247, and 0.614, respectively), while the RQ levels of TNF-α in the GC group were upregulated (RQ = 2.749), but were basal for IL-8 (RQ = 1.053) and downregulated for IL-10 (RQ = 0.179). When the groups were stratified according to wild-type and polymorphic alleles, only for IL-8-845 T/C the polymorphic allele was found to influence the expression levels of this cytokine. IL-8-845 C allele carriers were significantly upregulated in both groups (GC and CG; RQ = 3.138 and 2.181, respectively) when compared to TT homozygotes (RQ = -0.407 and 0.165, respectively). In silico analysis in the IL-8 promoter region revealed that the presence of the variant C allele in position -845 is responsible for the presence of the binding sites for two transcription factors (REL and CREB1), which are involved in increased gene expression. Polymorphic alleles were not shown to have any effect on the expression levels of TNF-α and IL-10. Taken together, our findings provide evidence for an association of TNF-α-857 C/T, IL-8-845 T/C, and IL-10-592 C/A with a higher risk of gastric cancer and also demonstrate the influence that the polymorphic C allele of IL-8-845 has on changes to the gene expression levels of this cytokine.en
dc.description.affiliationFaculdade de Medicina de São José do Rio Preto, Departamento de Genética e Biologia Molecular
dc.description.affiliationUnespUniversidade Estadual Paulista, Departamento de Biologia, Instituto de Biociências, Letras e Ciências Exatas de São José do Rio Preto
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2010/00507-0
dc.description.sponsorshipIdCNPq: 471908/2010-0
dc.identifierhttp://dx.doi.org/10.1007/s13277-015-3593-x
dc.identifier.citationTumour Biology : The Journal Of The International Society For Oncodevelopmental Biology And Medicine, 2015.
dc.identifier.dimensionspub.1016995924
dc.identifier.doi10.1007/s13277-015-3593-x
dc.identifier.issn1423-0380
dc.identifier.issn1010-4283
dc.identifier.lattes7991082362671212
dc.identifier.orcid0000-0001-5693-6148
dc.identifier.orcid0000-0003-0959-0695
dc.identifier.orcid0000-0002-2125-9930
dc.identifier.orcid0000-0002-3476-2885
dc.identifier.orcid0000-0003-1814-8954
dc.identifier.orcid0000-0002-2622-4673
dc.identifier.orcid0000-0003-1491-8878
dc.identifier.pmid26088449
dc.identifier.pubmed26088449
dc.identifier.urihttp://hdl.handle.net/11449/131277
dc.language.isoeng
dc.publisherSpringer Nature
dc.relation.ispartofTumour Biology : The Journal Of The International Society For Oncodevelopmental Biology And Medicine
dc.relation.ispartofsjr1,149
dc.rights.accessRightsAcesso restritopt
dc.sourcePubMed
dc.sourceDimensions
dc.subjectChronic gastritisen
dc.subjectCytokinesen
dc.subjectGastric canceren
dc.subjectGene expressionen
dc.subjectGene polymorphismsen
dc.titleInfluence of functional polymorphisms in TNF-α, IL-8, and IL-10 cytokine genes on mRNA expression levels and risk of gastric canceren
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication43c38943-bd6f-4fb6-a9a5-8482a1f632c0
relation.isOrgUnitOfPublication.latestForDiscovery43c38943-bd6f-4fb6-a9a5-8482a1f632c0
unesp.author.lattes7991082362671212[8]
unesp.author.lattes2503906319038306[11]
unesp.author.orcid0000-0001-5693-6148[8]
unesp.author.orcid0000-0003-1491-8878[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentBiologia - IBILCEpt

Arquivos