Wang Chengyuan, Sturgis Erich M, Chen Xingming, Zheng Hongliang, Wei Qingyi, Li Guojun
Department of Otolaryngology-Head and Neck Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Oncotarget. 2016 May 3;7(18):26444-53. doi: 10.18632/oncotarget.8512.
Functional polymorphisms of miRNAs may affect the function and target expression of miRNAs, which can, in turn, affect the biological activity, etiology, and prognosis of cancer. We hypothesized that four common polymorphisms in pre-miRNAs (hsa-mir-146a rs2910164 G > C, hsa-mir-196a2 rs11614913 C > T, hsa-mir-149 rs2292832 G > T, and hsa-mir-499 rs3746444 A > G) are associated with survival in SCCNOP. We used univariate and multivariable Cox models to evaluate the associations between the four polymorphisms and survival. We found that hsa-mir-149 rs2292832 and hsa-mir-499 rs3746444 had statistically significant associations with survival, but hsa-mir-146a rs2910164 and hsa-mir-196a2 rs11614913 did not. Patients having the hsa-mir-149 CC and hsa-mir-499 TT wild-type genotypes had significantly better overall, disease-specific, and disease-free survival compared with those who had the corresponding variant CT/TT and CT/CC genotypes, respectively. Furthermore, these genotypes were significantly associated with reduced risk of overall death, death owing to disease, and recurrence after adjustment for important prognostic confounders, indicating that these pre-miRNA polymorphisms may be prognostic biomarkers for SCCNOP. Moreover, the stratified analyses based on smoking status and treatment indicated that the effects of hsa-mir-149 and hsa-mir-499 polymorphisms on survival were more pronounced in ever smokers and patients treated with chemoradiation. Our findings support that the hsa-mir-149 rs2292832 and hsa-mir-499 rs3746444 polymorphisms play a significant role in the prognosis of SCCNOP, especially in smokers and patients treated with chemoradiation. Prospective studies with larger sample sizes are needed to confirm these findings.
微小RNA(miRNA)的功能多态性可能会影响miRNA的功能和靶标表达,进而影响癌症的生物学活性、病因及预后。我们推测前体miRNA中的四个常见多态性位点(hsa-mir-146a rs2910164 G>C、hsa-mir-196a2 rs11614913 C>T、hsa-mir-149 rs2292832 G>T和hsa-mir-499 rs3746444 A>G)与口咽鳞状细胞癌(SCCNOP)的生存相关。我们使用单变量和多变量Cox模型来评估这四个多态性位点与生存之间的关联。我们发现,hsa-mir-149 rs2292832和hsa-mir-499 rs3746444与生存具有统计学意义上的显著关联,但hsa-mir-146a rs2910164和hsa-mir-196a2 rs11614913则不然。与分别具有相应变异型CT/TT和CT/CC基因型的患者相比,具有hsa-mir-149 CC和hsa-mir-499 TT野生型基因型的患者的总生存、疾病特异性生存和无病生存均显著更好。此外,在对重要的预后混杂因素进行校正后,这些基因型与总死亡风险、疾病相关死亡风险和复发风险的降低显著相关,这表明这些前体miRNA多态性位点可能是SCCNOP的预后生物标志物。此外,基于吸烟状态和治疗的分层分析表明,hsa-mir-149和hsa-mir-499多态性对生存的影响在曾经吸烟者和接受放化疗的患者中更为明显。我们的研究结果支持hsa-mir-149 rs2292832和hsa-mir-499 rs3746444多态性在SCCNOP的预后中起重要作用,尤其是在吸烟者和接受放化疗的患者中。需要更大样本量的前瞻性研究来证实这些发现。