Department of Hepatology, Zaozhuang Municipal Hospital, Zaozhuang, Sandong, China.
Department of Cardiovascular Medicine, Zaozhuang Municipal Hospital, Zaozhuang, Shandong, China.
Biochem Biophys Res Commun. 2020 May 7;525(3):581-588. doi: 10.1016/j.bbrc.2020.02.116. Epub 2020 Feb 27.
Long non-coding RNAs (lncRNAs) have obtained growing attention due to their potential effects as novel regulators in various tumors. This study aimed to investigate the expression and roles of lncRNA LINC01139 (LINC01139) in the progression of hepatocellular carcinoma (HCC). We found that LINC01139 was over-expressed in HCC specimens and cell lines, and its upregulation was observed to be associated with advanced TNM stage, lymph node metastasis and poor clinical prognosis of HCC patients. Multivariate analyses confirmed that LINC01139 expression was an independent poor prognostic factor for HCC patients. Functionally, the knockdown of LINC01139 suppressed cell proliferation, clone formation and metastasis of HCC cells. Moreover, luciferase assays and rescue experiments revealed that LINC01139/miR-30/MYBL2 established the ceRNA network involved in the modulation of cell proliferation and metastasis of HCC cells. Overall, LINC01139 may exhibit an oncogenic function in HCC via acting as a sponge for miR-30 to upregulate MYBL2, and may serve as a potential therapeutic target and a prognostic biomarker for HCC patients.
长链非编码 RNA(lncRNA)因其作为各种肿瘤新型调节剂的潜在作用而受到越来越多的关注。本研究旨在探讨 lncRNA LINC01139(LINC01139)在肝细胞癌(HCC)进展中的表达和作用。我们发现 LINC01139 在 HCC 标本和细胞系中过度表达,其上调与 HCC 患者的晚期 TNM 分期、淋巴结转移和不良临床预后相关。多变量分析证实 LINC01139 表达是 HCC 患者的独立不良预后因素。功能上,敲低 LINC01139 抑制了 HCC 细胞的增殖、克隆形成和转移。此外,荧光素酶测定和挽救实验表明,LINC01139/miR-30/MYBL2 建立了 ceRNA 网络,参与调节 HCC 细胞的增殖和转移。总之,LINC01139 可能通过作为 miR-30 的海绵来上调 MYBL2 在 HCC 中发挥致癌作用,并且可以作为 HCC 患者的潜在治疗靶点和预后生物标志物。