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

. 2021 Apr 9;11:639980. doi: 10.3389/fonc.2021.639980

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

Copyright © 2021 Zhang, Jiang, Wang, Cheng and Fu.

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 function of LIPE-AS1/miR-195-5p in cervical cancer cells. (A) MiR-195-5p mimics and inhibitors were taken to construct miR-195-5p over- and down-expressing cell lines, respectively, and further transfected with LIPE-AS1 over-expressed plasmids or sh-LIPE-AS1 to perform compensation experiments. CCK8 method (B) and BrdU method (C) were employed to detect HeLa and HCC94 cell proliferation. (D) Flow cytometry was performed to test the apoptosis of HeLa and HCC94 cells. (E) Transwell method was carried out to examine HeLa and HCC94 cell invasion. The expressions of E-cadherin, Snail, and Vimentin in HeLa (F) and HCC94 cells (G) were examined by Western blot. **P < 0.01, ***P < 0.001 vs. Vector or sh-NC group. ^&P < 0.05, ^&&P < 0.01, ^&&&P < 0.001 vs. LIPE-AS1 group or sh-LIPE -AS1 group. N = 3.