Department of Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.
Mol Carcinog. 2013 Nov;52 Suppl 1:E10-8. doi: 10.1002/mc.21931. Epub 2012 Jun 12.
Genetic variants in micro-RNAs (miRNA) have been shown to affect progression, diagnosis, and prognosis of various malignancies; however, their role in esophageal squamous cell carcinoma (ESCC) susceptibility is controversial. Therefore, we aimed to determine role of common genetic variants in cancer related pre-miRNA in susceptibility and survival outcome of north Indian ESCC patients. We genotyped four common polymorphisms in pre-miRNA: mir-196a-2C>T, mir-146aG>C, mir-499T>C, and mir-423C>A in 289 incident ESCC cases (including 153 follow-up cases) and 309 controls using PCR/PCR RFLP-based methods. Binary logistic regression was applied for risk estimation, while Kaplan-Meier and Cox Regression tests were performed for survival analysis. We observed that none of the pre-miRNA genetic variants were associated with ESCC or its clinical phenotypes independently, however, combined risk genotypes of four pre-miRNA polymorphisms increased risk of ESCC in dose-response manner (Ptrend = 0.011). Specifically, patients with 2-4 risk genotypes of pre-miRNA polymorphisms had 1.4-fold higher risk of ESCC compared to patients with 0-1 risk genotypes (OR = 1.43, 95% CI = 1.02-1.09, P-value = 0.037). The risk was more pronounced in ESCC cases with upper-third esophageal tumors. Moreover, cumulative but not independent effect of risk genotypes of pre-miRNA polymorphisms was observed on survival outcome of ESCC patients. Cases with 2-4 risk genotypes had significantly lower median survival (11.60 vs. 30.2 months) and 2.3-fold greater hazard of death compared to patients with 0-1 risk genotypes. In conclusion, the four studied common pre-miRNA polymorphisms cumulatively affect susceptibility and survival of ESCC patients in north Indian population. © 2012 Wiley Periodicals, Inc.
miRNA 中的遗传变异已被证明会影响各种恶性肿瘤的进展、诊断和预后;然而,它们在食管鳞状细胞癌(ESCC)易感性中的作用仍存在争议。因此,我们旨在确定常见癌症相关 miRNA 前体 miRNA 中的遗传变异在北印度 ESCC 患者易感性和生存结局中的作用。我们使用 PCR/PCR RFLP 方法对 289 例新发病例 ESCC 患者(包括 153 例随访病例)和 309 例对照中的四个 miRNA 前体 miRNA 中的常见多态性:mir-196a-2C>T、mir-146aG>C、mir-499T>C 和 mir-423C>A 进行了基因分型。二元逻辑回归用于风险估计,而 Kaplan-Meier 和 Cox 回归检验用于生存分析。我们发现,miRNA 前体遗传变异均与 ESCC 或其临床表型无关,但四种 miRNA 前体多态性的联合风险基因型以剂量反应方式增加 ESCC 的风险(Ptrend = 0.011)。具体而言,与 0-1 个风险基因型相比,具有 2-4 个 miRNA 多态性风险基因型的患者发生 ESCC 的风险增加了 1.4 倍(OR = 1.43,95%CI = 1.02-1.09,P 值 = 0.037)。在上三分之一食管肿瘤的 ESCC 病例中,这种风险更为明显。此外,还观察到 miRNA 前体多态性风险基因型对 ESCC 患者生存结局的累积而非独立影响。具有 2-4 个风险基因型的病例中位生存时间显著缩短(11.60 与 30.2 个月),死亡风险增加 2.3 倍。总之,在北印度人群中,研究的四个常见 miRNA 前体多态性共同影响 ESCC 患者的易感性和生存。