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miRNA 中的遗传变异可预测膀胱癌风险和复发。

Genetic variants in miRNAs predict bladder cancer risk and recurrence.

机构信息

State Key Laboratory of Reproductive Medicine, Institute of Toxicology, Nanjing Medical University, 140 Hanzhong Road, Nanjing 210029, China.

出版信息

Cancer Res. 2012 Dec 1;72(23):6173-82. doi: 10.1158/0008-5472.CAN-12-0688. Epub 2012 Jul 30.

Abstract

miRNAs play important roles in numerous cellular processes, including development, proliferation, apoptosis, and carcinogenesis. Because altered expression and function of miRNAs has been observed in bladder cancer, we investigated whether genetic variations in miRNAs are associated with bladder cancer risk and prognosis. Using bioinformatics tools, we selected five single-nucleotide polymorphisms located in miRNAs and used these to evaluate miRNA-disease associations in a two-stage model, consisting of 1,019 bladder cancer cases and 1,182 controls (683 cases and 728 controls in the training set and 336 cases and 454 controls in the test set). We found that miR-146a rs2910164 C allele was associated with significantly decreased risk of bladder cancer in both the training and test sets, as well as the combined set [OR = 0.80, 95% confidence interval (CI) = 0.71-0.90, P = 2.92 × 10(-4)]. Furthermore, the rs2910164 GC/CC genotypes conferred a significantly reduced risk of recurrence, compared with the GG genotype (P = 0.016). Functional analysis revealed that miR-146a rs2910164 C allele inhibited cell proliferation and significantly downregulated expression of IRAK1 and TRAF6 in bladder cancer cells. Additional examination of 64 bladder cancer tissues showed that individuals carrying the C allele had increased expression levels of miR-146a compared with those carrying the G allele (P = 0.010). Taken together, our findings show that miR-146a rs2910164 plays an important role in the risk and recurrence of bladder cancer, suggesting it may represent a biomarker for risk prevention and therapeutic intervention. Further larger and prospective cohorts are needed to validate our findings.

摘要

miRNAs 在许多细胞过程中发挥重要作用,包括发育、增殖、凋亡和致癌作用。由于在膀胱癌中观察到 miRNAs 的表达和功能改变,我们研究了 miRNAs 的遗传变异是否与膀胱癌风险和预后相关。使用生物信息学工具,我们选择了位于 miRNAs 中的五个单核苷酸多态性,并使用这些多态性在两阶段模型中评估 miRNA-疾病关联,该模型由 1019 例膀胱癌病例和 1182 例对照组成(训练集中有 683 例病例和 728 例对照,测试集中有 336 例病例和 454 例对照)。我们发现,miR-146a rs2910164 的 C 等位基因与膀胱癌的风险显著降低相关,无论是在训练集还是测试集,以及合并组中[OR=0.80,95%置信区间(CI)=0.71-0.90,P=2.92×10(-4)]。此外,与 GG 基因型相比,rs2910164 GC/CC 基因型显著降低了复发风险(P=0.016)。功能分析表明,miR-146a rs2910164 的 C 等位基因抑制了膀胱癌细胞的增殖,并显著下调了 IRAK1 和 TRAF6 的表达。对 64 例膀胱癌组织的进一步检查表明,携带 C 等位基因的个体与携带 G 等位基因的个体相比,miR-146a 的表达水平升高(P=0.010)。总之,我们的研究结果表明,miR-146a rs2910164 在膀胱癌的风险和复发中起着重要作用,表明它可能代表着预防风险和治疗干预的生物标志物。需要进一步进行更大和前瞻性的队列研究来验证我们的发现。

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