miR-499 rs3746444 and miR-196a-2 rs11614913 Are Associated with the Risk of Glioma, but Not the Prognosis

Bibliographic Details
Title: miR-499 rs3746444 and miR-196a-2 rs11614913 Are Associated with the Risk of Glioma, but Not the Prognosis
Authors: Si Yang, Yi Zheng, Linghui Zhou, Jing Jin, Yujiao Deng, Jia Yao, Pengtao Yang, Li Yao, Ying Wu, Zhen Zhai, Na Li, Lijuan Lyu, Zhijun Dai
Source: Molecular Therapy: Nucleic Acids, Vol 22, Iss , Pp 340-351 (2020)
Publisher Information: Elsevier, 2020.
Publication Year: 2020
Collection: LCC:Therapeutics. Pharmacology
Subject Terms: glioma, miR-499, miR-196a-2, single nucleotide polymorphism, susceptibility, survival, Therapeutics. Pharmacology, RM1-950
More Details: Previous studies of correlations of microRNA (miR)-499 rs3746444 and miR-196a-2 rs11614913 polymorphisms with glioma risk have yielded inconsistent results. In this study, relationships between these two polymorphisms and glioma risk and survival were evaluated. In total, 605 patients and 1,300 controls were genotyped. rs3746444 increased glioma risk in five genetic models (GA versus AA, odds ratio [OR], 95% confidence interval [CI] = 1.31 [1.05–1.66], p = 0.02; GG versus AA, OR [95% CI] = 10.70 [6.13–18.69], p < 0.0001; GA + GG versus AA, OR [95% CI] = 1.82 [1.47–2.24], p < 0.0001; GG versus AA + GA, OR [95% CI] = 9.99 [5.74–17.40], p < 0.0001; G versus A, OR [95% CI] = 2.18 [1.82–2.60], p < 0.0001). rs11614913 decreased glioma risk in a recessive model (OR [95% CI] = 0.79 [0.64–0.97], p = 0.03). No relationships between either SNP and survival were found. rs3746444 in the miR-499 seed region could affect target recognition. Bioinformatics analyses indicated that miR-499 rs3746444 is involved in various biological processes and pathways, including “cell adhesion molecule binding,” “positive regulation of catabolic process,” “NF-kappa B pathway,” and “PI3K-Akt pathway,” by targeting mRNAs. Our results suggested that miR-499 rs3746444 and miR-196a-2 rs11614913 have crucial roles in glioma susceptibility.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2162-2531
Relation: http://www.sciencedirect.com/science/article/pii/S2162253120302687; https://doaj.org/toc/2162-2531
DOI: 10.1016/j.omtn.2020.08.038
Access URL: https://doaj.org/article/4cbe97d7b635445db9ac834d06003ca6
Accession Number: edsdoj.4cbe97d7b635445db9ac834d06003ca6
Database: Directory of Open Access Journals
More Details
ISSN:21622531
DOI:10.1016/j.omtn.2020.08.038
Published in:Molecular Therapy: Nucleic Acids
Language:English