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 Dec 18;20:167. doi: 10.1186/s12943-021-01474-9

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

© The Author(s) 2021

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 — circIL4R facilitates the proliferation, migration and invasion of CRC cells in vitro. a and b qRT-PCR validation of circIL4R and IL4R mRNA expression in HCT116 and LoVo cells transfected with siRNAs and overexpression plasmids, respectively. c and d The viability curves of CRC cells with knockdown or overexpression of circIL4R were detected by the CCK-8 assay at the indicated time points. e and f A colony formation assay was conducted to determine the proliferation of CRC cells stably transfected with sh-Ctrl, sh- circIL4R, vector or circIL4R. g and h An EdU assay was performed to assess the proliferation ability of CRC cells transfected with the indicated siRNAs or plasmids. i to l Representative images and quantification of Transwell and wound healing assays of CRC cells transfected with the indicated siRNAs or plasmids. The data are presented as the mean ± SD. *P < 0.05, **P < 0.01, ***P < 0.001