Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2022 Jul 22;12:927706. doi: 10.3389/fonc.2022.927706

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2022 Mo, Hu, Yang, Li, Bashir, Nai, Ma, Jia and Xu

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

PMC Copyright notice

The effect of lncRNA MIR31HG on lung adenocarcinoma LUAD cell viability, migration, and invasion. (A) The efficiency of MIR31HG knockdown (si-MIR31HG-1 and si-MIR31HG-2) was assessed by qRT-PCR. (B) The subcellular localization of MIR31HG was predicted by “LncLocator”. (C, D) The relative lncRNA MIR31HG expression level both in the cytoplasm and the nucleus of the NCI-H2009 and A549 cell lines were simultaneously measured by qRT-PCR. (E, F) The proliferation of NCI-H2009 and A549 cells was detected by CCK-8 assays. (G, H) The invasion of NCI-H2009 and A549 cells was investigated by transwell assays. (I, J) The clone capacity of NCI-H2009 and A549 cells was identified by colony formation assay. (K, L) The migration of NCI-H2009 and A549 cells was determined by wound healing assays. ^* p < 0.05; ^** p < 0.01; ^*** p < 0.001.