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

. 2020 Aug 27;20:414. doi: 10.1186/s12935-020-01510-6

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

© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

PMC Copyright notice

Fig. 4 — MIR99AHG/miR-577/FOXP1 axis regulated the malignant phenotype of GC cells. a mRNA level of FOXP1 was confirmed by qPCR in BGC-823 and SGC-7901 cell following MIR99AHG knockdown, MIR99AHG overexpression, and MIR99AHG overexpression plus FOXP1 knockdown. b Protein expression level of FOXP1 was confirmed by western blot in BGC-823 and SGC-7901 cell following MIR99AHG knockdown, MIR99AHG overexpression, and MIR99AHG overexpression plus FOXP1 knockdown. c, d CCK8 proliferation assay in BGC-823 and SGC-7901 cells after MIR99AHG overexpression and MIR99AHG overexpression plus FOXP1 knockdown. e Trans-well assay shows invasion effect. f, g Qualification of the trans-well assay. h E-cadherin and N-cadherin expression levels were detected by Western blotting. *p < 0.05, **p < 0.01 and ***p < 0.001 (two-way ANOVA)