{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Torruella-Loran I"],"funding":["Fondo de Fomento al Desarrollo Científico y Tecnológico","Instituto de Salud Carlos III","“la Caixa” Foundation","Ministerio de Ciencia e Innovación","European Regional Development Fund"],"pagination":["e832"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6687864"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["7(8)"],"pubmed_abstract":["<h4>Background</h4>MicroRNAs are small regulatory RNAs with important roles in carcinogenesis. Genetic variants in these regulatory molecules may contribute to disease. We aim to identify allelic variants in microRNAs as susceptibility factors to gastric cancer using association studies and functional approaches.<h4>Methods</h4>Twenty-one single nucleotide variants potentially functional, because of their location in either the seed, mature or precursor region of 22 microRNAs, were selected for association studies. Genetic association with gastric cancer in 365 cases and 1,284 matched controls (European Prospective Investigation into Cancer and Nutrition Cohort) was analysed using logistic regression. MicroRNA overexpression, transcriptome analysis, and target gene validation experiments w"],"journal":["Molecular genetics & genomic medicine"],"pubmed_title":["rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene."],"pmcid":["PMC6687864"],"funding_grant_id":["FONDECYT 1170446","BM06-130-0","BFU2010-18477","PI070130 and PI12/01187"],"pubmed_authors":["Munoz X","Torruella-Loran I","Bonet C","Gonzalez CA","Garcia-Ramallo E","Espinosa-Parrilla Y","Sala N","Zapata-Contreras D","Ramirez Vina MK","EPIC gastric cancer working group"],"additional_accession":[]},"is_claimable":false,"name":"rs12416605:C>T in MIR938 associates with gastric cancer through affecting the regulation of the CXCL12 chemokine gene.","description":"<h4>Background</h4>MicroRNAs are small regulatory RNAs with important roles in carcinogenesis. Genetic variants in these regulatory molecules may contribute to disease. We aim to identify allelic variants in microRNAs as susceptibility factors to gastric cancer using association studies and functional approaches.<h4>Methods</h4>Twenty-one single nucleotide variants potentially functional, because of their location in either the seed, mature or precursor region of 22 microRNAs, were selected for association studies. Genetic association with gastric cancer in 365 cases and 1,284 matched controls (European Prospective Investigation into Cancer and Nutrition Cohort) was analysed using logistic regression. MicroRNA overexpression, transcriptome analysis, and target gene validation experiments w","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Aug","modification":"2026-04-08T05:56:34.468Z","creation":"2019-08-20T07:03:52Z"},"accession":"S-EPMC6687864","cross_references":{"pubmed":["31273931"],"doi":["10.1002/mgg3.832"]}}