Hepatitis B virus X protein related lncRNA WEE2-AS1 promotes hepatocellular carcinoma proliferation and invasion

被引:35
|
作者
Hu, Zhigang [1 ,2 ,3 ]
Huang, Pinbo [2 ]
Yan, Yongcong [1 ,2 ]
Zhou, Zhenyu [1 ,2 ]
Wang, Jie [2 ]
Wu, Gang [4 ]
机构
[1] Sun Yat Sen Univ, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Med Res Ctr, Sun Yat Sen Mem Hosp, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Hepatobiliary Surg, Sun Yat Sen Mem Hosp, Guangzhou, Guangdong, Peoples R China
[3] Nanchang Univ, Dept Hepatobiliary Surg, Affiliated Hosp 2, Nanchang, Jiangxi, Peoples R China
[4] Univ Elect Sci & Technol China, Dept Hepatobiliary Surg, Sichuan Prov Peoples Hospital, 32 Yihuan Rd, Chengdu 610072, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; Long non-coding RNA; Hepatitis B virus x protein; WEE2-AS1; FERMT3; LONG NONCODING RNAS; MOLECULAR-MECHANISMS; CELL-PROLIFERATION; LIVER-CANCER; EXPRESSION; METASTASIS; CONTRIBUTES; INTEGRATION; REPRESSION;
D O I
10.1016/j.bbrc.2018.11.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis B virus X protein (HBx) is involved in the initiation and progression of hepatocellular carcinoma (HCC) by regulating the host protein-coding genes. In this study, we showed that HBx altered the expression of lncRNAs to promote the progression of HCC. lncRNA microarray and quantitative reverse-transcription polymerase chain reactions (qRT-PCRs) were performed to identify lncRNAs that were differentially regulated by HBx in HCC cells and tissues. Protein, mRNA, and lncRNA expression analyses; cell cycle and apoptosis analyses; loss/gain-of-function analysis were performed to delineate the consequences of WEE2-AS1 upregulation in HCC cells. WEE2-AS1 over-expressed in HCC and was positively correlated to hepatitis B virus (HBV) infection, hepatic vascular invasion, poor tumor differentiation and poor patient prognosis. WEE2-AS1 also accelerated the proliferation, migration, invasion and cell cycle progression of HCC cells. Fermitin family member 3 (FERMT3) was a downstream target of WEE2-AS1. In conclusion, there is a preliminary HBx-WEE2-AS1- FERMT3 pathway which may serve as a therapeutic target for HBV-associated HCC. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:79 / 86
页数:8
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