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Prognostic Role of microRNA-205 in Human Gynecological Cancer: A Meta-Analysis of Fourteen Studies

机译:MicroRNA-205在人类妇科癌症中的预后作用:十四研究的荟萃分析

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摘要

Several studies have revealed that miR-205 plays important roles in the development of gynecological cancers and thus may serve as a potential prognostic biomarker, but the current conclusions remain controversial. Therefore, the goal of this study was to explore the prognostic significance and functional mechanisms of miR-205 based on a meta-analysis and bioinformatics investigation. A total of 14 published studies containing 5835 patients were enrolled by searching the PubMed, EMBASE, and Cochrane library databases, 13 (14 datasets) and 5 (6 datasets) of which evaluated the correlations between the expression level of miR-205 and overall survival (OS) or disease-free survival (DFS)/disease-specific survival (DSS)/progression-free survival (PFS)/distant metastasis-free survival (DMFS), respectively. Furthermore, the use of online Kaplan-Meier plotter database analysis supplemented another seven results for OS. Then, a meta-analysis using these 21 and 6 datasets was performed. As a result, the overall analysis failed to demonstrate any significant associations between miR-205 expression and OS (p = 0.267) or DSS/DFS/DMFS/PFS (p = 0.457), but the subgroup analysis suggested that elevated miR-205 predicted a reduced OS for breast cancer (BC) patients (hazard ratio [HR] = 0.84, 95% confidence interval [CI] = 0.72-0.98; p = 0.022), while higher miR-205 was associated with a poor DSS for endometrial cancer (EC) patients (HR = 2.19, 95% CI = 1.45-3.32; p < 0.001). Function prediction analysis indicated that miR-205 may be involved in BC by negatively influencing hub genes, SMARCA5 and SIAH1, whereas miR-205 may participate in EC by negatively modulating BMPR1B because of the presence of interactions of miR-205 with them at 3 '-untranslated region and their opposite prognosis outcomes with miR-205. In conclusion, our findings suggest miR-205 may be a promising prognostic biomarker and therapeutic target for BC and EC patients.
机译:若干研究表明,MIR-205在妇科癌症的发展中起重要作用,因此可能用作潜在的预后生物标志物,但目前的结论仍然存在争议。因此,本研究的目的是探讨MIR-205基于Meta分析和生物信息学研究的预后显着性和功能机制。通过搜索Pubmed,Embase和Cochrane库数据库,13(14个数据集)和5(6个数据集),共注册了14项含有5835名患者的发布研究,其中评估了MiR-205的表达水平与总体生存之间的相关性(OS)或无病生存(DFS)/疾病特异性存活(DSS)/无进展的存活(PFS)/远离转移的存活(DMF)。此外,使用在线Kaplan-Meier绘图仪数据库分析为OS提供了另外七个结果。然后,执行使用这些21和6个数据集的元分析。结果,整体分析未能展示MIR-205表达和OS(P = 0.267)或DSS / DFS / DMFS / PFS(P = 0.457)之间的任何显着关联,但亚组分析表明提升MIR-205预测乳腺癌(BC)患者的减少操作系统(危害比[HR] = 0.84,95%置信区间[CI] = 0.72-0.98; p = 0.022),而较高的miR-205与用于子宫内膜癌的差的DSS相关(EC)患者(HR = 2.19,95%CI = 1.45-3.32; P <0.001)。功能预测分析表明,MIR-205可以通过影响轮毂基因,SMARCA5和SIAH1来涉及BC,而MIR-205可以通过对BMPR1B进行负调节BMPR1B来参与EC,因为MIR-205与它们在3'上与它们相互作用。 - 用miR-205,淘汰的地区及其对其对立预后的结果。总之,我们的研究结果表明MIR-205可能是BC和EC患者的有希望的预后生物标志物和治疗靶标。

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