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Comprehensive Analysis of the Expression Profiles of Long Non-Coding RNAs with Associated ceRNA Network Involved in the Colon Cancer Staging and Progression

机译:结肠癌分期和进展中涉及相关的Cerna网络的长编码RNA表达谱的综合分析

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Long non-coding RNAs (lncRNAs) act as competing endogenous RNAs (ceRNAs) to compete with microRNAs (miRNAs) in cancer occurrence and development. However, the differential expression of RNAs and their ceRNA network during the development of colon cancer (CC) remains unclear. This study was aimed at comprehensive analysis of the lncRNAs and their ceRNA networks associated with CC. Whole transcriptome sequencing was performed on colorectal and adjacent normal tissues at different pathological stages. Forty-nine lncRNAs were differently expressed between the CC tissues and their adjacent normal tissues at all stages. Aberrant expression of lncRNA CDKN2B-AS1 and lncRNA MIR4435-2HG was confirmed by TCGA database. Moreover, 14 lncRNAs were differentially expressed between early and advance stages of the tumor tissues, and 117 miRNAs were specifically expressed in stage III & IV. Weighted gene co-expression network analysis of 17105 differently expressed mRNAs revealed that the mRNAs shown in module pink, midnight blue, black, and light cyan were related to TNM and pathological stage, and that these mRNAs were enriched in cancer related functions and pathways. As DElncRNA showed a trend of change similar to that of the DEmRNA and opposite to that of DEmiRNA, ceRNA network was constructed with 3 DEmiRNAs, 5 DElncRNAs, and 130 DEmRNAs. Real time PCR revealed that expression of MEG3 was decreased in the tumor tissues belonging to stage III and IV as compared to that in stage I. Moreover, hsa-miR-324-5p was upregulated, while FGFR3, PLCB4, and IKBKB were downregulated in the tumor tissues as compared to that in the adjacent normal tissues. Thus, this study revealed differentially expressed lncRNA between different stages of CC as well as suggested that lncRNA CDKN2B-AS1, MIR4435-2HG, and MEG3 may act as diagnostic biomarkers for the development of CC.
机译:长期非编码RNA(LNCRNA)作为竞争内源性RNA(CERNAS),以与癌症发生和发展中的微小RNA(miRNA)竞争。然而,在结肠癌(CC)开发期间RNA和它们的Cerna网络的差异表达仍不清楚。本研究旨在综合分析与CC相关的LNCRNA及其CERNA网络。在不同病理阶段对结直肠和相邻的正常组织进行整个转录组测序。在CC组织和所有阶段的CC组织和相邻的正常组织之间不同地表达四十九个LNCRNA。 TCGA数据库证实了LNCRNA CDKN2B-AS1和LNCRNA miR4435-2Hg的异常表达。此外,在肿瘤组织的早期和预先阶段之间差异表达了14个LNCRNA,在III阶段和IV中特异性地表达了117mIRNA。 17105的加权基因共表达网络分析不同表达MRNA显示,模块粉红色,午夜蓝,黑色和浅色青色中所示的MRNA与TNM和病理阶段有关,并且这些MRNA富含癌症相关功能和途径。由于DelncrNa显示出类似于DEMRNA的变化的趋势,与DemiRNA的变化相反,Cerna网络用3个DemiRNA,5 delncrna和130 demrnas构建。实时PCR揭示了在属于III阶段和IV的肿瘤组织中,MEG3的表达减少,与IS阶段I中相比,HSA-MIR-324-5P被上调,而FGFR3,PLCB4和IKBKB在下调与相邻正常组织中的肿瘤组织相比。因此,该研究揭示了CC的不同阶段之间的差异表达的LNCRNA,并且表明LNCRNA CDKN2B-AS1,miR4435-2Hg和MEG3可以作为CC发育的诊断生物标志物。

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