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Genetic variation in MicroRNA genes and risk of oral premalignant lesions

✍ Scribed by Jessica Clague; Scott M. Lippman; Hushan Yang; Michelle A.T. Hildebrandt; Yuanqing Ye; J. Jack Lee; Xifeng Wu


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
79 KB
Volume
49
Category
Article
ISSN
0899-1987

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✦ Synopsis


Abstract

MicroRNAs (miRNAs) have been reported to play a key role in oncogenesis and, recently, studies have examined the role miRNAs might play in the risk of premalignant lesions. To our knowledge, no study has investigated the association between miRNA polymorphisms and risk of oral premalignant lesions (OPLs). We genotyped 31 single nucleotide polymorphisms (SNPs) among 21 miRNA‐related genes in a case–control study including 136 OPL patients and 136 matched controls. Patients with at least one variant allele of __mir26a‐1:__rs7372209 had a significantly increased risk of OPL (OR, 2.09; 95% CI, 1.23–3.56). Likewise, patients with at least one variant allele of DICER:rs3742330 had a significantly increased risk of OPL (OR, 2.09; 95% CI, 1.03–4.24). To assess the cumulative effects, we performed a combined unfavorable genotype analysis that included all SNPs showing at least a borderline statistical significance. A significant trend of increased risk of OPL with increasing number of unfavorable genotypes was observed (P for trend <0.0001). This study presents the first epidemiologic evidence supporting that individual as well as combined genotypes of miRNA‐related variants may be used to predict the risk of OPL, and may be useful for identifying patients with OPL at high risk for progression to oral cancer. Β© 2009 Wiley‐Liss, Inc.


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