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首页> 外文期刊>Expert Review of Molecular Diagnostics >A microRNA meta-signature for pancreatic ductal adenocarcinoma.
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A microRNA meta-signature for pancreatic ductal adenocarcinoma.

机译:胰腺导管腺癌的microRNA meta-signature。

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Due to its aggressive and late presentation, there is an urgent need for novel and reliable biomarkers for the diagnosis and prognostication of pancreatic ductal adenocarcinoma (PDAC). MiRNAs have been extensively profiled in PDAC tissues, biopsies, blood samples and other biofluids and their expression levels compared to normal and chronic pancreatitis (CP) specimens in order to identify the most relevant candidates. Consolidation of these activities has not been attempted until now. The evaluated meta-review by Ma et al. helps to define the use of miRNAs as biomarkers for detecting this tumor-type and predicting survival outcomes in PDAC. Based on frequency and consistency between microarray studies, they identified a miRNA meta-signature for recognising PDAC: upregulation of miR-21, 23a, 31, 100, 143, 155, and 221; with downregulation of miR-148a, 217 and 375. Furthermore, they validated high miR-21, high miR-31 and low miR-375 tumoural expression as independently prognostic for poor overall-survival (OS; n = 70).
机译:由于其侵袭性和晚期表现,迫切需要新颖且可靠的生物标志物用于胰腺导管腺癌(PDAC)的诊断和预后。 MiRNA在PDAC组织,活组织检查,血液样本和其他生物流体中已被广泛地分析,并且与正常和慢性胰腺炎(CP)标本相比,它们的表达水平是最高的。到目前为止,尚未尝试合并这些活动。 Ma等人评估的元审查。帮助定义miRNA作为生物标记物的用途,以检测这种肿瘤类型并预测PDAC的生存结果。基于微阵列研究之间的频率和一致性,他们确定了识别PDAC的miRNA元特征:miR-21、23a,31、100、143、155和221的上调;随着miR-148a,217和375的下调。此外,他们确认高miR-21,高miR-31和低miR-375肿瘤表达可独立预测整体生存不良(OS; n = 70)。

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