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Authordc.contributor.authorFavaro Trombone, Ana Paula 
Authordc.contributor.authorCavalla Ruiz, Ian Franco 
Authordc.contributor.authorVarize Silveira, Elcia María 
Authordc.contributor.authorAndreo, Camile Bermejo 
Authordc.contributor.authorFrancisconi, Carolina Favaro 
Authordc.contributor.authorFonseca, Angélica Cristina 
Authordc.contributor.authorLetra, Ariadne 
Authordc.contributor.authorSilva, Renato Menezes 
Authordc.contributor.authorGarlet, Gustavo Pompermaier 
Admission datedc.date.accessioned2017-03-01T19:11:05Z
Available datedc.date.available2017-03-01T19:11:05Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationJournal of Applied Oral Science. Volumen: 24 Número: 4 Páginas: 366-375es_ES
Identifierdc.identifier.other10.1590/1678.775720160112
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/142834
Abstractdc.description.abstractIncreased matrix metalloproteinases (MMPs) activity is a hallmark of periapical granulomas. However, the factors underlying the MMPs expression modulation in healthy and diseased periapical tissues remains to be determined. Objective: In this study, we evaluated the association between the MMP1-1607 polymorphism (rs1799750) and pro-inflammatory milieu elements with MMP-1 mRNA levels in vivo. Material and Methods: MMP1-1607 SNP and the mRNA levels of MMP-1, TNF-alpha, IFN-gamma, IL-17A, IL-21, IL-10, IL-4, IL-9, and FOXp3 were determined via RealTimePCR in DNA/RNA samples from patients presenting periapical granulomas (N=111, for both genotyping and expression analysis) and control subjects (N=214 for genotyping and N=26 for expression analysis). The Shapiro-Wilk, Fisher, Pearson, Chi-square ordinal least squares regression tests were used for data analysis (p<0.05 was considered statistically significant). Results: The MMP1-1607 1G/2G and 1G/2G+2G/2G genotypes were significantly more prevalent in the patients than in controls, comprising a risk factor for periapical lesions development. MMP-1 mRNA levels were higher in periapical lesions than in healthy periodontal ligament samples, as well as higher in active than in inactive lesions. The polymorphic allele 2G carriers presented a significantly higher MMP-1 mRNA expression when compared with the 1G/1G genotype group. The ordered logistic regression demonstrated a significant correlation between the genetic polymorphism and the expression levels of MMP-1. Additionally, the pro- and anti-inflammatory cytokines IL-17A, IFN-gamma, TNF-alpha, IL-21, IL-10, IL-9, and IL-4 were significant as complementary explanatory variables of MMP-1 expression. Conclusion: The MMP1-1607 SNP was identified as a risk factor for periapical lesions development, possibly due to its association with increased MMP-1 mRNA levels in periapical lesions. The MMP-1 expression is also under the control of the inflammatory milieu elements, being the cytokines TNF-alpha, IL-21, IL-17A, and IFN-g associated with increased MMP-1 levels in periapical lesions, while IL-10, IL-9, or IL-4 presented an inverse association.es_ES
Lenguagedc.language.isoenes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceJournal of Applied Oral Sciencees_ES
Keywordsdc.subjectCytokineses_ES
Keywordsdc.subjectInflammationes_ES
Keywordsdc.subjectGenetices_ES
Keywordsdc.subjectPolymorphismes_ES
Keywordsdc.subjectMatrix metalloproteinaseses_ES
Keywordsdc.subjectPeriapical granulomaes_ES
Keywordsdc.subjectPeriapical diseaseses_ES
Títulodc.titleMMP1-1607 polymorphism increases the risk for periapical lesion development through the upregulation MMP-1 expression in association with pro-inflammatory milieu elementses_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorC. R. B.es_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile