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The diagnostic/prognostic potential and molecular functions of long non-coding RNAs in the exosomes derived from the bile of human cholangiocarcinoma

机译:人胆管癌胆汁来源的外泌体中长非编码RNA的诊断/预后潜力和分子功能

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摘要

Cholangiocarcinoma (CCA) is an aggressive malignancy associated with unfavorable prognosis, and it’s difficult to diagnose and no effective treatments are available. Long non-coding RNAs (lncRNAs) play important roles in tumorigenesis and metastasis. Intact lncRNAs from exosomes have sparked much interest as potential biomarker for the non-invasive analysis of disease. Here, via exosome sequencing on lncRNAs, GO analysis, KEGG pathway and co-expression analysis, receiver operating characteristic curve and survival analyses, we found that, compared with control group, lncRNAs of ENST00000588480.1 and ENST00000517758.1 showed significantly increased expressions in CCA group. Moreover, area under the curve (AUC) was increased to 0.709 when combined the two lncRNAs, they had a sensitivity and specificity of 82.9% and 58.9% respectively. Further, the higher levels of the two lncRNAs showed a significantly increasing trend with the advancement of cancer TNM stages, and prognosticated a poor survival. In addition, KEGG pathway analysis showed that the most significant difference term was “p53 signaling pathway” (KEGG ID: hsa04115, p: 0.001). The altered lncRNAs and their target genes were included to reconstruct a co-expression network. These altered lncRNAs were mainly related to cellular processes, environmental information processing and organismal systems, etc. Collectively, our findings provided the potential roles of lncRNAs of ENST00000588480.1 and ENST00000517758.1 in CCA, and implicated these lncRNAs as potential diagnostic and therapeutic targets for CCA.
机译:胆管癌(CCA)是一种侵袭性恶性肿瘤,预后不良,难以诊断,尚无有效的治疗方法。长的非编码RNA(lncRNA)在肿瘤发生和转移中起重要作用。来自外来体的完整lncRNAs引起了人们极大的兴趣,将其作为疾病非侵入性分析的潜在生物标记。在这里,通过对lncRNA的外来体测序,GO分析,KEGG途径和共表达分析,受体工作特征曲线和存活分析,我们发现,与对照组相比,ENST00000588480.1和ENST00000517758.1的lncRNAs的表达明显增加。 CCA组。此外,当组合两个lncRNA时,曲线下面积(AUC)增加至0.709,它们的敏感性和特异性分别为82.9%和58.9%。此外,随着癌症TNM分期的进展,两种lncRNA的较高水平显示出明显增加的趋势,并且预后不良。此外,KEGG通路分析显示,最显着的差异是“ p53信号通路”(KEGG ID:hsa04115,p:0.001)。改变的lncRNA及其靶基因被包括在内以重建共表达网络。这些改变的lncRNA主要与细胞过程,环境信息处理和生物系统等相关。我们的发现共同提供了ENST00000588480.1和ENST00000517758.1的lncRNA在CCA中的潜在作用,并暗示了这些lncRNA作为潜在的诊断和治疗靶标用于CCA。

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