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The correlation of circulating pro‐angiogenic miRNAs’ expressions with disease risk clinicopathological features and survival profiles in gastric cancer

机译:循环中促血管生成miRNA的表达与胃癌的疾病风险临床病理特征和生存状况的相关性

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摘要

This study aimed to explore the correlation of circulating pro‐angiogenic miRNAs’ expressions with risk, clinicopathological features, and survival profiles in gastric cancer (GC). Three hundred and thirty‐three GC patients underwent radical resection and 117 health controls (HCs) were recruited for this study. Plasma samples were obtained from GC patients before the operation and from HCs after enrollment. Fourteen pro‐angiogenic miRNAs were asseassed by quantitative polymerase chain reaction (qPCR). Disease‐free survival (DFS) and overall survival (OS) of GC patients were calculated and the median follow‐up duration was 36.0 months. Seven out of 14 pro‐angiogenic miRNAs including let‐7f, miR‐17‐5p, miR‐18a, miR‐19b‐1, miR‐20a, miR‐210, and miR‐296 were observed to be elevated in GC patients compared with HCs. MiR‐18a, miR‐20a, and miR‐210 disclosed good predictive values of GC risk. Six pro‐angiogenic miRNAs including miR‐17‐5p, miR‐92a, miR‐210, miR‐20a, miR‐18a, and miR‐296 expressions were positively while 1 pro‐angiogenic mi style="fixed-case">RNA (miR‐130a) was negatively correlated with tumor malignancy degree in style="fixed-case">GC patients. K‐M curve disclosed that 5 pro‐angiogenic mi style="fixed-case">RNAs including miR‐17‐5p, miR‐18a, miR‐20a, miR‐92a, and miR‐210 correlated with worse style="fixed-case">DFS, while 4 pro‐angiogenic mi style="fixed-case">RNAs including miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 associated with shorter style="fixed-case">OS. Further multivariate Cox's analysis revealed that miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 were independent predictive factors for unfavorable style="fixed-case">DFS and style="fixed-case">OS. In conclusion, circulating pro‐angiogenic mi style="fixed-case">RNAs could serve as novel noninvasive biomarkers for disease risk and malignancy degree, and miR‐17‐5p, miR‐18a, miR‐20a, and miR‐210 are independent factors predicting poor prognosis in style="fixed-case">GC patients.
机译:这项研究旨在探讨循环中促血管生成的miRNA表达与胃癌(GC)的风险,临床病理特征和生存特征之间的关系。 333例接受根治性切除术的GC患者接受了117例健康对照(HCs)的研究。术前从GC患者和入组后的HC中获取血浆样品。通过定量聚合酶链反应(qPCR)评估了14种促血管生成性miRNA。计算出GC患者的无病生存期(DFS)和总生存期(OS),中位随访时间为36.0个月。在GC患者中,观察到14种促血管生成性miRNA中的7种(包括let-7f,miR-17-5p,miR-18a,miR-19b-1,miR-20a,miR210和miR-296)升高与HC。 MiR-18a,miR-20a和miR-210揭示了GC风险的良好预测值。包括miR-17-5p,miR-92a,miR-210,miR-20a,miR-18a和miR-296在内的6种促血管生成miRNA阳性,而1种促血管生成mi style =“ fixed-case” > RNA (miR-130a)与 style =“ fixed-case”> GC 患者的恶性程度呈负相关。 K‐M曲线揭示了5个促血管生成mi style =“ fixed-case”> RNA ,包括miR-17-5p,miR-18a,miR-20a,miR-92a和miR-210与更差的 style =“ fixed-case”> DFS 相关,而4个促血管生成的mi style =“ fixed-case”> RNA s包括miR-17-5p,miR- 18a,miR-20a和miR-210与较短的 style =“ fixed-case”> OS 相关联。进一步的Cox多变量分析表明,miR-17-5p,miR-18a,miR-20a和miR-210是不利于 style =“ fixed-case”> DFS 和 style = “ fixed-case”>操作系统。总之,循环的促血管生成mi style =“ fixed-case”> RNA s可以作为疾病风险和恶性程度的新型非侵入性生物标记,以及miR-17-5p,miR-18a,miR- 20a和miR-210是预测 style =“ fixed-case”> GC 患者预后不良的独立因素。

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