LncRNA WDFY3-AS2 suppresses proliferation and invasion in oesophageal squamous cell carcinoma by regulating miR-23555p/SOCS2 axis

被引:28
作者
Zhang, Qing [1 ]
Guan, Fangxia [1 ]
Fan, Tianli [2 ]
Li, Shenglei [3 ]
Ma, Shanshan [1 ]
Zhang, Yanting [1 ]
Guo, Wenna [1 ]
Liu, Hongtao [1 ]
机构
[1] Zhengzhou Univ, Sch Life Sci, 100 Kexue Rd, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Sch Basic Med, Dept Pharmacol, Zhengzhou, Peoples R China
[3] Zhengzhou Univ, Dept Pathol, Affiliated Hosp 1, Zhengzhou, Peoples R China
关键词
ceRNA mechanism; invasion and metastasis; microRNA-2355-5p; oesophageal squamous cell carcinoma; suppressors of cytokine signalling 2; WDFY3-AS2; LONG NONCODING RNA; HEPATOCELLULAR-CARCINOMA; COLORECTAL-CANCER; PROGRESSION; EXPRESSION; CHEMORADIOTHERAPY; SOCS2; METASTASIS; BIOGENESIS; APOPTOSIS;
D O I
10.1111/jcmm.15488
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long non-coding RNAs (lncRNAs) widely participate in ESCC development and progression; however, the prognostic factors and therapeutic strategies implicated in ESCC development and progression remain to be under investigation. The purpose of the current study was to explore whether WDFY3-AS2 may be a potential prognostic factor and investigate its biological functions in ESCC. Here, WDFY3-AS2 was frequently down-regulated in ESCC tissues and cells, and its expression was correlated with TNM stage, lymph node metastasis and poor prognosis of ESCC patients. Moreover, WDFY3-AS2 down-regulation significantly promoted cell proliferation and invasion, whereas WDFY3-AS2 up-regulation markedly suppressed cell proliferation and invasion in ESCC EC9706 and TE1 cells, coupled with EMT phenotype alterations. WDFY3-AS2 functioned as a competing endogenous RNA (ceRNA) for sponging miR2355-5p, further resulted in the up-regulation of its target gene SOCS2, followed by suppression of JAK2/Stat5 signalling pathway, to suppress ESCC cell proliferation and invasion in EC9706 and TE1 cells. These findings suggest that WDFY3-AS2 may participate in ESCC development and progression, and may be a novel prognostic factor for ESCC patients, and thus targeting WDFY3-AS2/miR-2355-5p/SOCS2 signalling axis may be a novel therapeutic strategy for ESCC patients.
引用
收藏
页码:8206 / 8220
页数:15
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