Li Tangjian, Li Shengli, Chen Di, Chen Bing, Yu Tao, Zhao Fangyu, Wang Qifeng, Yao Ming, Huang Shenglin, Chen Zhiao, He Xianghuo
Fudan University Shanghai Cancer Center and Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, China.
State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cancer Sci. 2017 May;108(5):877-885. doi: 10.1111/cas.13209. Epub 2017 Apr 26.
RNA-binding proteins (RBPs) play fundamental roles in the RNA life cycle. The aberrant expression of RBPs is often observed in human disease, including cancer. In this study, we screened for the expression levels of 1542 human RBPs in The Cancer Genome Atlas liver hepatocellular carcinoma samples and found 92 consistently upregulated RBP genes in HCC compared with normal samples. Additionally, we undertook a Kaplan-Meier analysis and found that high expression of 15 RBP genes was associated with poor prognosis in patients with HCC. Furthermore, we found that eIF3c promotes HCC cell proliferation in vitro as well as tumorigenicity in vivo. Gene Set Enrichment Analysis showed that high eIF3c expression is positively associated with KRAS, vascular endothelial growth factor, and Hedgehog signaling pathways, all of which are closely associated with specific cancer-related gene sets. Our study provides the basis for further investigation of the molecular mechanism by which eIF3c promotes the development and progression of HCC.
RNA结合蛋白(RBPs)在RNA生命周期中发挥着重要作用。RBPs的异常表达在包括癌症在内的人类疾病中经常被观察到。在本研究中,我们在癌症基因组图谱的肝细胞癌样本中筛选了1542种人类RBPs的表达水平,发现与正常样本相比,肝癌中有92个RBP基因持续上调。此外,我们进行了Kaplan-Meier分析,发现15个RBP基因的高表达与肝癌患者的不良预后相关。此外,我们发现eIF3c在体外促进肝癌细胞增殖,并在体内促进肿瘤发生。基因集富集分析表明,eIF3c的高表达与KRAS、血管内皮生长因子和Hedgehog信号通路呈正相关,所有这些都与特定的癌症相关基因集密切相关。我们的研究为进一步研究eIF3c促进肝癌发生发展的分子机制提供了依据。