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miRNA 和 mRNA 的综合分析支持结直肠癌的二十个 miRNA 特征。

Integrated Analysis of miRNA and mRNA Endorses a Twenty miRNAs Signature for Colorectal Carcinoma.

机构信息

Istituto di Ricerca Genetica e Biomedica (IRGB), CNR, Cittadella Universitaria di Cagliari, 09042 Monserrato (CA), Italy.

CRS4, Science and Technology Park Polaris, Piscina Manna, 09050 Pula (CA), Italy.

出版信息

Int J Mol Sci. 2019 Aug 20;20(16):4067. doi: 10.3390/ijms20164067.

Abstract

Colorectal cancer (CRC) ranks as the most frequent carcinoma worldwide. CRC patients show strong prognostic differences and responses to treatment, and 20% have incurable metastatic disease at diagnosis. We considered it essential to investigate mechanisms that control cellular regulatory networks, such as the miRNA-mRNA interaction, known to be involved in cancer pathogenesis. We conducted a human miRNome analysis by TaqMan low density array, comparing CRC to normal colon tissue (NCT, and experimentally identified gene targets of miRNAs deregulated, by anti-correlation analysis, with the CRC whole-transcriptome profile obtained from RNASeq experiments. We identified an integrated signature of 20 deregulated miRNAs in CRC. Enrichment analyses of the gene targets controlled by these miRNAs brought to light 25 genes, members of pathways known to lead to cell growth and death ( etc.), such as cell metabolism (). A screening of prognosis-mediated miRNAs underlined that the overexpression of miR-224 promotes CRC metastasis, and is associated with high stage and poor survival. These findings suggest that the biology and progression of CRC depend on deregulation of multiple miRNAs that cause a complex dysfunction of cellular molecular networks. Our results have further established miRNA-mRNA interactions and defined multiple pathways involved in CRC pathogenesis.

摘要

结直肠癌(CRC)是全球最常见的癌症之一。CRC 患者的预后和治疗反应存在明显差异,20%的患者在诊断时已发生无法治愈的转移性疾病。因此,研究控制细胞调控网络的机制至关重要,如 miRNA-mRNA 相互作用,该机制已知与癌症发病机制有关。我们通过 TaqMan 低密度阵列进行了人类 miRNome 分析,将 CRC 与正常结肠组织(NCT)进行比较,并通过反相关分析,从 RNA-seq 实验中获得 CRC 全转录组图谱,确定了 miRNA 失调的基因靶点。我们鉴定出 CRC 中存在 20 个失调 miRNA 的综合特征。对这些 miRNA 调控的基因靶点进行富集分析,揭示了 25 个基因,它们是已知导致细胞生长和死亡等途径的成员(如细胞代谢)。对预后介导的 miRNA 的筛选表明,miR-224 的过表达促进 CRC 转移,与高分期和不良预后相关。这些发现表明 CRC 的生物学和进展依赖于多个 miRNA 的失调,导致细胞分子网络的复杂功能障碍。我们的研究结果进一步确立了 miRNA-mRNA 相互作用,并确定了参与 CRC 发病机制的多个途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b64/6720928/34fbc6e4ec81/ijms-20-04067-g001.jpg

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