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ABSTRACT:
Methods: Sanger sequencing was used to analyze genotypes of lncRNA SNHG16 gene rs7353, rs8038, and rs15278 sites. Multifactor dimensionality reduction was used to analyze interactions between lncRNA SNHG16 gene rs7353, rs8038, rs15278 sites, and environmental factors. Haploview 4.1 software was used to analyze linkage disequilibrium of lncRNA SNHG16 gene rs7353, rs8038, and rs15278 sites. Quantitative real-time polymerase chain reaction was used to analyze plasma lncRNA SNHG16 levels of CRC patients and control subjects.
Results: Variation of the lncRNA SNHG16 gene rs7353 site A>G variation was associated with decreased CRC susceptibility (Odds ratio [OR]?=?0.50, 95% confidence interval [CI]: 0.40-0.62, P?A and rs15278 site A>G variation were associated with increased CRC susceptibility (OR?=?1.87, 95% CI: 1.47-2.36, P?A variation was associated with increased CRC susceptibility (OR?=?2.24, 95% CI: 1.61-3.11, P?G variation caused a significant decrease in plasma lncRNA SNHG16 level (P?A variation and rs15278 site A>G variation resulted in increased plasma lncRNA SNHG16 levels.
Conclusion: Polymorphisms of lncRNA SNHG16 gene rs7353, rs8038, rs15278 loci and their interaction with age are significantly associated with CRC susceptibility.
SUBMITTER: Zhou L
PROVIDER: S-EPMC7710222 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature
Zhou Li L Zhang Yuefeng Y Jin Jianjiang J Gu Xuewei X
Medicine 20201101 48
<h4>Objective</h4>To study the relationship between long-chain non-coding RNA small nucleolar RNA host gene 16 (lncRNA SNHG16) polymorphisms and its interaction with environmental factors and susceptibility to colorectal cancer (CRC).<h4>Methods</h4>Sanger sequencing was used to analyze genotypes of lncRNA SNHG16 gene rs7353, rs8038, and rs15278 sites. Multifactor dimensionality reduction was used to analyze interactions between lncRNA SNHG16 gene rs7353, rs8038, rs15278 sites, and environmental ...[more]