The IncRNA ZEB2-AS1 is upregulated in gastric cancer and affects cell proliferation and invasion via miR-143-5p/HIF-1α axis

被引:52
作者
Wu, Fangxiong [1 ]
Gao, Hongyan [1 ]
Liu, Kaige [1 ]
Gao, Baohua [1 ]
Ren, Hezhuang [1 ]
Li, Zheng [2 ]
Liu, Fengrui [2 ]
机构
[1] Xian Med Univ, Affiliated Hosp 1, Dept Gastroenterol, Xian, Shaanxi, Peoples R China
[2] Xian Med Univ, Affiliated Hosp 1, Dept Emergency, Fenghao West Rd 48, Xian 710077, Shaanxi, Peoples R China
关键词
gastric cancer; ZEB2-AS1; miR-143-5p; HIF-1; alpha; cell proliferation; metastasis; HYPOXIA-INDUCIBLE FACTOR; NONCODING RNAS; HIF-1-ALPHA; PROGRESSION; MIGRATION; PROGNOSIS; LNCRNAS;
D O I
10.2147/OTT.S175521
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Growing evidence has implicated the important role of the long non-coding RNAs (lncRNAs) in gastric cancer progression. In this study, we examined the expression of lncRNA zinc finger E-box-binding homeobox 2 antisense RNA 1 (ZEB2-AS1) in gastric cancer tissues and elucidated the molecular mechanisms underlying ZEB2-AS1-mediated gastric cancer progression. Methods: Quantitative real-time PCR measured the gene expression level; CCK-8, colony formation and cell invasion assays determined gastric cancer cell proliferation, growth and invasion, respectively; the xenograft nude mice model was used to determine in vivo tumor growth; Bioinformatics analysis and luciferase reporter assay determined the downstream targets of ZEB2-AS1 and miR-143-5p. The expression of ZEB2-AS1 was upregulated in gastric cancer cell lines. Results: Knockdown of ZEB2-AS1 suppressed gastric cancer cell proliferation, growth and invasion, and also suppressed in vivo tumor growth in the nude mice. Overexpression of ZEB2-AS1 potentiated gastric cancer cell proliferation, growth and invasion. Bioinformatics analysis and luciferase reporter assay showed that miR-143-5p was a direct target of ZEB2-AS1 and was negatively regulated by ZEB2-AS1. Furthermore, hypoxia-inducible factor-1 alpha (HIF-1 alpha) was found to be a target of miR-143-5p and was negatively regulated by miR-143-5p. The rescue in vitro assays showed that the effects of ZEB2-AS1 overexpression on gastric cancer cell proliferation, growth and invasion was mediated via miR-143-5p/HIF-1 alpha. ZEB2-AS1 and HIF-1 alpha was upregulated in gastric cancer tissues, while miR-143-5p was down-regulated; and ZEB2-AS1 expression level was inversely correlated with miR-143-5p expression level, and positively correlated with HIF-1 alpha mRNA expression level; while miR-143-5p expression level was inversely correlated with HIF-1 alpha expression level. High ZEB2-AS1 expression level was correlated with poor differentiation, lymph node metastasis and distant metastasis. Conclusion: Collectively, our results indicated that ZEB2-AS1 was up-regulated in gastric cancer tissues and cells and promoted cell proliferation and metastasis through miR-143-5p/HIF-1 alpha pathway, which may provide a promising target for treatment of gastric cancer.
引用
收藏
页码:657 / 667
页数:11
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