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表达HBx的肝细胞中microRNA和mRNA表达谱的综合分析。

Integrated analysis of microRNA and mRNA expression profiles in HBx-expressing hepatic cells.

作者信息

Chen Ruo-Chan, Wang Juan, Kuang Xu-Yuan, Peng Fang, Fu Yong-Ming, Huang Yan, Li Ning, Fan Xue-Gong

机构信息

Ruo-Chan Chen, Juan Wang, Yong-Ming Fu, Yan Huang, Xue-Gong Fan, Hunan Key Laboratory of Viral Hepatitis, Department of Infectious Disease, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.

出版信息

World J Gastroenterol. 2017 Mar 14;23(10):1787-1795. doi: 10.3748/wjg.v23.i10.1787.

Abstract

AIM

To identify the miRNA-mRNA regulatory network in hepatitis B virus X (HBx)-expressing hepatic cells.

METHODS

A stable HBx-expressing human liver cell line L02 was established. The mRNA and miRNA expression profiles of L02/HBx and L02/pcDNA liver cells were identified by RNA-sequencing analysis. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis was performed to investigate the function of candidate biomarkers, and the relationship between miRNA and mRNA was studied by network analysis.

RESULTS

Compared with L02/pcDNA cells, 742 unregulated genes and 501 downregulated genes were determined as differentially expressed in L02/HBx cells. Gene ontology analysis suggested that the differentially expressed genes were relevant to different biological processes. Concurrently, 22 differential miRNAs were also determined in L02/HBx cells. Furthermore, integrated analysis of miRNA and mRNA expression profiles identified a core miRNA-mRNA regulatory network that is correlated with the carcinogenic role of HBx.

CONCLUSION

Collectively, the miRNA-mRNA network-based analysis could be useful to elucidate the potential role of HBx in liver cell malignant transformation and shed light on the underlying molecular mechanism and novel therapy targets for hepatocellular carcinoma.

摘要

目的

鉴定表达乙型肝炎病毒X蛋白(HBx)的肝细胞中的miRNA-mRNA调控网络。

方法

建立稳定表达HBx的人肝细胞系L02。通过RNA测序分析鉴定L02/HBx和L02/pcDNA肝细胞的mRNA和miRNA表达谱。进行京都基因与基因组百科全书通路富集分析以研究候选生物标志物的功能,并通过网络分析研究miRNA与mRNA之间的关系。

结果

与L02/pcDNA细胞相比,确定742个上调基因和501个下调基因在L02/HBx细胞中差异表达。基因本体分析表明差异表达基因与不同生物学过程相关。同时,在L02/HBx细胞中也确定了22个差异miRNA。此外,miRNA和mRNA表达谱的综合分析确定了一个与HBx致癌作用相关的核心miRNA-mRNA调控网络。

结论

总体而言,基于miRNA-mRNA网络的分析有助于阐明HBx在肝细胞恶性转化中的潜在作用,并为肝细胞癌的潜在分子机制和新治疗靶点提供线索。

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