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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74807
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dc.contributor.authorJorge, Yvana Cristina-
dc.contributor.authorMataruco, Mayra Mioto-
dc.contributor.authorAraújo, Leandro Pires-
dc.contributor.authorRossi, Ana Flávia Teixeira-
dc.contributor.authorDe Oliveira, Juliana Garcia-
dc.contributor.authorValsechi, Marina Curado-
dc.contributor.authorCaetano, Alaor-
dc.contributor.authorMiyazaki, Kenji-
dc.contributor.authorFazzio, Célia Sebastiana de Jesus-
dc.contributor.authorThomé, Jorge Alberto-
dc.contributor.authorRahal, Paula-
dc.contributor.authorOliani, Sonia Maria-
dc.contributor.authorSilva, Ana Elizabete-
dc.date.accessioned2014-05-27T11:28:39Z-
dc.date.accessioned2016-10-25T18:45:32Z-
dc.date.available2014-05-27T11:28:39Z-
dc.date.available2016-10-25T18:45:32Z-
dc.date.issued2013-03-07-
dc.identifierhttp://dx.doi.org/10.1155/2013/152860-
dc.identifier.citationMediators of Inflammation, v. 2013.-
dc.identifier.issn0962-9351-
dc.identifier.issn1466-1861-
dc.identifier.urihttp://hdl.handle.net/11449/74807-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74807-
dc.description.abstractObjective. The anti-inflammatory proteins annexin-A1 and galectin-1 have been associated with tumor progression. This scenario prompted us to investigate the relationship between the gene and protein expression of annexin-A1 (ANXA1/AnxA1) and galectin-1 (LGALS1/Gal-1) in an inflammatory gastric lesion as chronic gastritis (CG) and gastric adenocarcinoma (GA) and its association with H. pylori infection. Methods. We analyzed 40 samples of CG, 20 of GA, and 10 of normal mucosa (C) by the quantitative real-time PCR (qPCR) technique and the immunohistochemistry assay. Results. High ANXA1 mRNA expression levels were observed in 90% (36/40) of CG cases (mean relative quantification RQ = 4.26 ± 2.03) and in 80% (16/20) of GA cases (mean RQ = 4.38 ± 4.77). However, LGALS1 mRNA levels were high (mean RQ = 2.44 ± 3.26) in 60% (12/20) of the GA cases, while low expression was found in CG (mean RQ = 0.43 ± 3.13; P < 0.01). Normal mucosa showed modest immunoreactivity in stroma but not in epithelium, while stroma and epithelium displayed an intense immunostaining in CG and GA for both proteins. Conclusion. These results have provided evidence that galectin-1 and mainly annexin-A1 are overexpressed in both gastritis and gastric cancer, suggesting a strong association of these proteins with chronic gastric inflammation and carcinogenesis. © 2013 Yvana Cristina Jorge et al.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectgalectin 1-
dc.subjectlipocortin 1-
dc.subjectmessenger RNA-
dc.subjectadult-
dc.subjectchronic gastritis-
dc.subjectcontrolled study-
dc.subjectdisease association-
dc.subjectfemale-
dc.subjectgene expression-
dc.subjectHelicobacter infection-
dc.subjectHelicobacter pylori-
dc.subjecthuman-
dc.subjecthuman cell-
dc.subjectimmunohistochemistry-
dc.subjectimmunoreactivity-
dc.subjectmajor clinical study-
dc.subjectmale-
dc.subjectpriority journal-
dc.subjectprotein expression-
dc.subjectreal time polymerase chain reaction-
dc.subjectstomach adenocarcinoma-
dc.subjectaged-
dc.subjectgastritis-
dc.subjectgenetics-
dc.subjectin vitro study-
dc.subjectmetabolism-
dc.subjectmiddle aged-
dc.subjectpathogenicity-
dc.subjectpathophysiology-
dc.subjectreverse transcription polymerase chain reaction-
dc.subjectstomach tumor-
dc.subjectAdult-
dc.subjectAged-
dc.subjectAnnexin A1-
dc.subjectFemale-
dc.subjectGalectin 1-
dc.subjectGastritis-
dc.subjectHelicobacter Infections-
dc.subjectHumans-
dc.subjectMale-
dc.subjectMiddle Aged-
dc.subjectReverse Transcriptase Polymerase Chain Reaction-
dc.subjectRNA, Messenger-
dc.subjectStomach Neoplasms-
dc.titleExpression of annexin-A1 and galectin-1 anti-inflammatory proteins and mRNA in chronic gastritis and gastric canceren
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionRio Preto Endoscopy Center-
dc.contributor.institutionHospital de Base-
dc.contributor.institutionInstitute of Anatomical Pathology and Cytopathology-
dc.description.affiliationDepartment of Biology São Paulo State University (UNESP) Campus de São José Do Rio Preto, Rua Cristóvão Colombo 2265, 15054-000 São José do Rio Preto, SP-
dc.description.affiliationRio Preto Endoscopy Center, São José do Rio Preto, SP-
dc.description.affiliationEndoscopy Service Hospital de Base, São José do Rio Preto, SP-
dc.description.affiliationLegal Medicine Department and Pathology Service Hospital de Base, São José do Rio Preto, SP-
dc.description.affiliationInstitute of Anatomical Pathology and Cytopathology, São José do Rio Preto, SP-
dc.description.affiliationUnespDepartment of Biology São Paulo State University (UNESP) Campus de São José Do Rio Preto, Rua Cristóvão Colombo 2265, 15054-000 São José do Rio Preto, SP-
dc.identifier.doi10.1155/2013/152860-
dc.identifier.wosWOS:000314583500001-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84874527295.pdf-
dc.relation.ispartofMediators of Inflammation-
dc.identifier.scopus2-s2.0-84874527295-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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