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Authordc.contributor.authorMorales, Sebastián
Authordc.contributor.authorGulppi, Felipe
Authordc.contributor.authorGonzález Hormazábal, Patricio
Authordc.contributor.authorFernández Ramires, Ricardo
Authordc.contributor.authorBravo, Teresa
Authordc.contributor.authorReyes, José
Authordc.contributor.authorPoblete Gómez, Fernando Andrés
Authordc.contributor.authorWaugh, Enrique
Authordc.contributor.authorJara Sosa, Lilian
Admission datedc.date.accessioned2016-11-30T21:07:22Z
Available datedc.date.available2016-11-30T21:07:22Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationBMC Genetics (2016) 17:109es_ES
Identifierdc.identifier.other10.1186/s12863-016-0415-0
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/141556
Abstractdc.description.abstractBackground: MicroRNAs (miRNAs) are a novel class of endogenous, non-coding, single-stranded RNAs capable of regulating gene expression by suppressing translation or degrading mRNAs. Single nucleotide polymorphisms (SNP) can alter miRNA expression, resulting in diverse functional consequences. Previous studies have examined the association of miRNA SNPs with breast cancer (BC) susceptibility. The contribution of miRNA gene variants to BC susceptibility in South American women had been unexplored. Our study evaluated the association of the SNPs rs895819 in pre-miR27a, rs11614913 in pre-miR-196a2, rs6505162 in pre-miR-423, rs4919510 in miR-608, and rs2682818 in pre-mir-618 with familial BC and early-onset non-familial BC in non-carriers of BRCA1/2 mutations from a South American population. Results: We evaluated the association of five SNPs with BC risk in 440 cases and 807 controls. Our data do not support an association of rs11614913:C > T and rs4919510:C > G with BC risk. The rs6505162:C > A was significantly associated with increased risk of familial BC in persons with a strong family history of BC (OR = 1.7 [95 % CI 1.0-2.0] p = 0.05). The rs2682818:C > A genotype C/A is associated with an increased BC risk in non-familial early-onset BC. For the rs895819: A > G polymorphism, the genotype G/G is significantly associated with reduced BC risk in families with a moderate history of BC (OR = 0.3 [95 % CI 0.1-0.8] p = 0.01). Conclusions: The contribution of variant miRNA genes to BC in South American women had been unexplored. Our findings support the following conclusions: a) rs6505162:C > A in pre-miR-423 increases risk of familial BC in families with a strong history of BC; b) the C/A genotype at rs2682818:C > A (pre-miR-618) increases BC risk in non-familial early-onset BC; and c) the G/G genotype at rs895819: A > G (miR-27a) reduces BC risk in families with a moderate history of BC.es_ES
Patrocinadordc.description.sponsorshipFondo Nacional de Desarrollo Cientifico y Tecnologico (FONDECYT) 1150117es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherBioMed Centrales_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.sourceBMC Geneticses_ES
Keywordsdc.subjectFamilial breast canceres_ES
Keywordsdc.subjectPolymorphismses_ES
Keywordsdc.subjectMicroRNAes_ES
Keywordsdc.subjectSouth American populationes_ES
Títulodc.titleAssociation of single nucleotide polymorphisms in Pre-miR-27a, Pre-miR- 196a2, Pre-miR-423, miR-608 and Pre-miR- 618 with breast cancer susceptibility in a South American populationes_ES
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso abierto
Catalogueruchile.catalogadorapces_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