Loss of lncRNA SNHG8 promotes epithelial-mesenchymal transition by destabilizing CDH1 mRNA

被引:5
作者
He, Ping
Zhang, Cheng
Chen, Guoqiang
Shen, Shaoming [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Key Lab Cell Differentiat & Apoptosis, Dept Pathophysiol,Chinese Minist Educ,Sch Med, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
SNHG8; epithelial-mesenchymal transition; CDH1; mRNA stability; E-CADHERIN; BREAST-CANCER; EXPRESSION; PROTEIN; EMT; METASTASIS; GENE; ENDOCYTOSIS; PROGRESSION; MIGRATION;
D O I
10.1007/s11427-020-1895-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Long non-coding RNAs (lncRNAs) are widely involved in a variety of biological processes, including epithelial-mesenchymal transition (EMT). In the current study, we found that lncRNA small nucleolar RNA host gene 8 (SNHG8) was tightly correlated with EMT-associated gene signatures, and was down-regulated by Zinc finger E-box-binding homeobox 1 (ZEB1) during EMT progress. Functionally, knockdown of SNHG8 induced EMT in epithelial cells, through destabilizing the CDH1 mRNA dependent on a 17-nucleotide sequence shared by SNHG8 and CDH1. In addition, analysis with public database showed that SNHG8 tended to be down-regulated in different cancer types and the lower expression of SNHG8 predicted poorer prognosis. Taken together, our study reports a ZEB1-repressed lncRNA SNHG8 which is important for stabilizing CDH1 mRNA, thereby maintaining the epithelial status of epithelial cells.
引用
收藏
页码:1858 / 1867
页数:10
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