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Published on: May 21, 2019
Genetic Variations in Key MicroRNAs are Associated With the Survival of Nonsmall Cell Lung Cancer
Shuangshuang Wu1, Wei Shen, Yun Pan
1From the Department of Geriatrics (SW, YL, WX, BC, JW); Editorial Department of Journal of Clinical Dermatology (YP); Department of Oncology, The First Affiliated Hospital of Nanjing Medical University (JX); Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University (WS, MZ, KX, LG, YW, ZH, HM); Jiangsu Key Lab of Cancer Biomarkers, Prevention and Treatment, Collaborative Innovation Center for Cancer Personalized Medicine, Nanjing Medical University (WS, MZ, KX, LG, YW, ZH, HM, HS); and State-Level Model Center of Experimental Teaching, Department of Hygienic Analysis and Detection, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu, P.R. China (SC).
Abstract:
MicroRNAs (miRNAs) are a class of small, noncoding RNA molecules involved in carcinogenesis. It has been identified that genetic variations in miRNAs contribute to cancer risk, prognosis, and survival. In the present study, we investigated whether single nucleotide polymorphisms (SNPs) of several key miRNAs (miR-184, miR-218, and miR-124) were associated with the prognosis of nonsmall cell lung cancer (NSCLC) in a clinical cohort study including 1001 cases. Cox proportional hazards regression models were used to estimate the hazard ratios (HRs) and their 95% confidence intervals (CIs). We found that 5 SNPs were associated with NSCLC survival (rs919968, rs3775815, rs4867902, and rs6122390 in an additive model: adjusted HR = 1.15, 95% CI = 1.02-1.29; adjusted HR = 0.78, 95% CI = 0.67-0.91, adjusted HR = 1.24, 95% CI = 1.09-1.41; adjusted HR = 1.21, 95% CI = 1.07-1.36, respectively; rs298206 in a dominant model: HR = 1.25, 95% CI = 1.05-1.49). Even after the Bonferroni correction, 3 SNPs remained significant (adjusted P = 0.010, 0.010, and 0.032 for rs3775815, rs4867902, and rs6122390, respectively). Additionally, the combined analysis of these 5 SNPs showed a significant locus-dosage effect between number of unfavorable alleles (rs919968-A, rs3775815-C, rs4867902-G, rs6122390-A, and rs298206-T) and death risk of NSCLC (P for trend < 0.001). A statistically significant multiplicative interaction was found between the genotypes of rs4867902 and surgical operation status (Pint = 0.013). These findings indicated that genetic variations in miRNAs (miR-184, miR-218, and miR-124) might be prognostic markers for NSCLC patients.
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