LncRNA GATA2-AS1 suppresses esophageal squamous cell carcinoma progression via the mir-940/PTPN12 axis

被引:9
|
作者
Niu, Yunfeng [1 ]
Guo, Yanli [1 ]
Li, Yan [1 ]
Shen, Supeng [1 ]
Liang, Jia [1 ]
Guo, Wei [1 ]
Dong, Zhiming [1 ,2 ]
机构
[1] Hebei Med Univ, Hebei Canc Inst, Lab Pathol, Hosp 4, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Hebei Canc Inst, Hosp 4, Jiankang Rd 12, Shijiazhuang 050011, Hebei, Peoples R China
关键词
LncRNAs; GATA2-AS1; miR-940; PTPN12; ceRNA; CANCER; PTPN12; ESCC; PROLIFERATION; MIGRATION;
D O I
10.1016/j.yexcr.2022.113130
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Esophageal squamous cell carcinoma (ESCC) is a common malignant tumor worldwide. Long noncoding RNAs (lncRNAs) exhibit a regulatory role in the progression of ESCC. Our research was performed to investigate the potential molecular mechanism of lncRNA GATA2-AS1 in ESCC. Methods: The expression of GATA2-AS1 was identified by qRT-PCR. Cell function assays explored the potential effect of GATA2-AS1 on ESCC progression. The subcellular hierarchical localization method was executed to identify the subcellular localization of GATA2AS1 in ESCC cells. A prediction website was utilized to discover the relationships among GATA2-AS1, miR-940 and PTPN12. Dual luciferase reporter gene, pull-down assays and RIP assays were executed to verify the binding activity among GATA2-AS1, miR-940 and PTPN12. Xenograft tumor experiments were performed to evaluate ESCC cell growth in vivo. Results: The expression of GATA2-AS1 and PTPN12 was reduced, while miR-940 expression was enhanced in ESCC tissues and cell lines. In vivo experiments showed that GATA2-AS1 inhibited the progression of ESCC cells toward malignancy. Bioinformatics analysis, dual luciferase and RIP assays revealed that GATA2-AS1 upregulated PTPN12 expression by competitively targeting miR-940. miR-940 reversed the inhibitory effect of GATA2-AS1 on the biological behavior of ESCC cells. Conclusion: Our findings suggested that GATA2-AS1, expressed at low levels in ESCC, plays a crucial role in the progression of ESCC by targeting the miR-940/PTPN12 axis and could be a potential drug target to treat ESCC patients.
引用
收藏
页数:12
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