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靶向染色体开放阅读框基因的异常微小RNA在肝癌循环来源的微泡中富集。

Abnormal miRNAs Targeting Chromosome Open Reading Frame Genes were Enriched in Microvesicles Derived from the Circulation of HCC.

作者信息

Lu Li, Guo Dongmei, Chen Xiaomei, Xiong Wei, Jie Shenghua, Li Huiyu

机构信息

Center for Stem Cell Research and Application, Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Affiliated Hospital of Jining Medical College, Jining, Shandong, China.

出版信息

Biochem Genet. 2016 Apr;54(2):120-33. doi: 10.1007/s10528-015-9705-x. Epub 2015 Nov 28.

Abstract

In this study, we detected the expression profiles of microRNAs (miRNAs) packaged within microvesicles (MVs) from blood samples of HCC patients and healthy donors. Using microarray analysis, there were 83 down-regulated and 92 over-expressed miRNAs in HCC circulation-derived MVs relative to control group. Then potential functions of the dysregulated MVs miRNAs were investigated with bioinformatic tools. We found that 664 Corf genes were targeted by 72 altered MVs miRNAs and some of these target genes were reported to be associated with tumorous activities. Gene Ontology annotation demonstrated that biological roles of the target Corf genes mainly contained the regulation of growth, cell death, macromolecule metabolism, etc. As regulated by abnormal MVs miRNAs, functions of target Corf genes might be interrupted, which were much likely to contribute to HCC occurrence and progression.

摘要

在本研究中,我们检测了肝癌患者和健康供体血液样本中微泡(MVs)内包装的微小RNA(miRNAs)的表达谱。通过微阵列分析,相对于对照组,肝癌循环来源的MVs中有83种miRNAs下调,92种miRNAs上调。然后,利用生物信息学工具研究了失调的MVs miRNAs的潜在功能。我们发现72种改变的MVs miRNAs靶向664个Corf基因,其中一些靶基因据报道与肿瘤活动相关。基因本体注释表明,靶Corf基因的生物学作用主要包括生长调节、细胞死亡、大分子代谢等。受异常MVs miRNAs调控,靶Corf基因的功能可能被中断,这很可能促成肝癌的发生和进展。

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