标题:A Preliminary Investigation of PVT1 on the Effect and Mechanisms of Hepatocellular Carcinoma: Evidence from Clinical Data, a Meta-Analysis of 840 Cases, and In Vivo Validation
作者:Zhang, Yu; Wen, Dong-yue; Zhang, Rui; Huang, Jia-cheng; Lin, Peng; Ren, Fang-Hui; Wang, Xiao; He, Yun; Yang, Hong; Chen, Gang; Luo 更多
作者机构:[Zhang, Yu; Zhang, Rui; Huang, Jia-cheng; Ren, Fang-Hui; Chen, Gang; Luo, Dian-Zhong] Guangxi Med Univ, Dept Pathol, Affiliated Hosp 1, Nanning, Peopl 更多
通讯作者:Yang, H;Chen, G
通讯作者地址:[Yang, H; Chen, G]Guangxi Med Univ, Affiliated Hosp 1, Dept Pathol & Med Ultrason, Guangxi 530021, Zhuang Autonomo, Peoples R China.
来源:CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
出版年:2018
卷:47
期:6
页码:2216-2232
DOI:10.1159/000491534
关键词:Pvt1; Hepatocellular carcinoma; TCGA; GEO; CAM; MiR-424-5p; INCENP
摘要:Background/Aims: Hepatocellular carcinoma (HCC) remains a difficult problem that significantly affects the survival of the afflicted patients. Accumulating evidence has demonstrated the functions of long non-coding RNA (lncRNA) in HCC. In the present study, we aimed to explore the potential roles of PVT1 in the tumorigenesis and progression of HCC. Methods: In this study, quantitative reverse transcription-polymerase chain reaction (RT-qPCR) was applied to detect the differences between PVT1 expression in HCC tissues and cell lines. Then, the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases were searched to confirm the relationship between PVT1 expression and HCC. Moreover, a meta-analysis comprising TCGA, GEO, and RT-qPCR was applied to estimate the expression of PVT1 in HCC. Then, cell proliferation was evaluated in vitro. A chicken chorioallantoic membrane (CAM) model of HCC was constructed to measure the effect on tumorigenicity in vivo. To further explore the sponge microRNA (miRNA) of PVT1 in HCC, we used TCGA, GEO, a gene microarray, and target prediction algorithms. TCGA and GEO and the gene microarray were used to select the differentially expressed miRNAs, and the different target prediction algorithms were applied to predict the target miRNAs of PVT1. Results: We found that PVT1 was markedly overexpressed in HCC tissue than in normal liver tissues based on both RT-qPCR and data from TCGA, and the overexpression of PVT1 was closely related to the gender and race of the patient as well as to higher HCC tumor grades. Also, a meta-analysis of 840 cases from multiple sources (TCGA, GEO and the results of our in-house RT-qPCR) showed that PVT1 gained moderate value in discriminating HCC patients from normal controls, confirming the results of RT-qPCR. Additionally, the upregulation of PVT1 could promote HCC cell proliferation in vitro and vivo. Based on the competing endogenous RNA (ceRNA) theory, the PVT1/miR-424-5p/INCENP axis was finally selected for further research. The in silico prediction revealed that there were complementary sequences between PVT1 and miR424-5p as well as between miR-424-5p and INCENP. Furthermore, a negative correlation trend was found between miR-424-5p and PVT1 based on RT-qPCR, whereas a positive correlation trend was found between PVT1 and INCENP based on data from TCGA. Also, INCENP small interfering RNA (siRNA) could significantly inhibit cell proliferation and viability. Conclusions: We hypothesized that PVT1 could affect the biological function of HCC cells via targeting miR424-5p and regulating INCENP. Focusing on the new insight of the PVT1/miR-424-5p/INCENP axis, this study provides a novel perspective for HCC therapeutic strategies. (C) 2018 The Author(s) Published by S. Karger AG, Basel
收录类别:SCOPUS;SCIE
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85049888535&doi=10.1159%2f000491534&partnerID=40&md5=e5bdd4fa500bf59ed1cde1f3c53f3dea
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