Litcius/Paper detail

Long noncoding RNA SBF2-AS1 contributes to the growth and metastatic phenotypes of NSCLC via regulating miR-338-3p/ADAM17 axis

Qi Chen, Sheng Min Guo, Hou Qiang Huang, Guo Huang, Yi Li, Zi Hui Li, Run Huang, Lu Xiao, Chun Rong Fan, Qing Yuan, Shouwen Zheng

2020Aging16 citationsDOIOpen Access PDF

Abstract

. Consistently, SBF2-AS1 knockdown hindered the growth of NSCLC cell in nude mice. The following luciferase reporter gene assay and RNA immunoprecipitation (RIP) assay suggested the relationship between miR-338-3p and SBF2-AS1. The rescue experiments showed that miR-338-3p inhibitor abolished SBF2-AS1 silencing caused inhibition on the growth, migration and invasiveness of NSCLC cell. The luciferase reporter assay and immunoblotting assay validated that A Disintegrin and Metalloprotease 17 (ADAM17) was a target of miR-338-3p. In addition, SBF2-AS1 positively regulated the level of ADAM17 through sponging for miR-338-3p. Finally, we revealed that SBF2-AS1 contributed to the proliferation and metastatic phenotypes of NSCLC cell via regulating miR-338-3p/ADAM17 axis.

Topics & Concepts

Gene knockdownGene silencingCancer researchBiologyPhenotypeLong non-coding RNAmicroRNACell growthMetastasisLuciferaseRNAGeneCancerTransfectionGeneticsCancer-related molecular mechanisms researchCircular RNAs in diseasesMicroRNA in disease regulation