| Literature DB >> 30272362 |
Yuanhong Chang1, Jie Zhang2, Cancan Zhou3, Guanglin Qiu4, Guanghui Wang4, Shufeng Wang4, Xinming Chang1, Xuqi Li4, Lin Fan4.
Abstract
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.Entities:
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Year: 2018 PMID： 30272362 DOI： 10.3892/or.2018.6752
Source DB: PubMed Journal: Oncol Rep ISSN： 1021-335X Impact factor: 3.906