Long non-coding RNA FOXD2-AS1 plays an oncogenic role in hepatocellular carcinoma by targeting miR-206

被引:39
|
作者
Chang, Yuanhong [1 ,2 ]
Zhang, Jie [3 ]
Zhou, Cancan [4 ]
Qiu, Guanglin [5 ]
Wang, Guanghui [5 ]
Wang, Shufeng [5 ]
Chang, Xinming [1 ]
Li, Xuqi [5 ]
Fan, Lin [5 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Gastroenterol, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Med, Affiliated Guangren Hosp, Dept Gastroenterol,Xian Hosp 4, Xian 710004, Shaanxi, Peoples R China
[3] Shaanxi Prov Tumor Hosp, Dept Gen Surg 1, Xian 710068, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Xian 710061, Shaanxi, Peoples R China
[5] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Gen Surg, 277 West Yanta Rd, Xian 710061, Shaanxi, Peoples R China
关键词
long non-coding RNA; FOXD2-AS1; microRNA; hepatocellular carcinoma; miR-206; PROMOTES; CANCER; CERNA; PROGRESSION; INVASION; PATHWAY;
D O I
10.3892/or.2018.6752
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recently, long non-coding RNA (lncRNA) FOXD2 adjacent opposite strand RNA 1 (FOXD2-AS1) has been recognized to function as an oncogene in several human tumors, and FOXD2-AS1 dysregulation has been closely associated with carcinogenesis and tumor progression. Nevertheless, the correlation between the aberrant expression of FOXD2-AS1 and the prognosis of hepatocellular carcinoma (HCC) has not yet been elucidated. In the present study, FOXD2-AS1 was found to be overexpressed in HCC tissues, and FOXD2-AS1 overexpression resulted in significantly shortened patient survival. FOXD2-AS1 overexpression enhanced the viability and metastasis of HCC cells in vitro and in vivo, as revealed by MTT, wound healing and cell migration assays. In addition, mechanistic studies revealed that FOXD2-AS1 upregulated the expression of the miR-206 target gene annexin A2 (ANXA2) by acting as a miR-206 sponge. In summary, FOXD2-AS1 was concluded to function as an oncogene in HCC and to upregulate ANXA2 expression in part by sponging' miR-206.
引用
收藏
页码:3625 / 3634
页数:10
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