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

. 2019 Apr 30;9:6652. doi: 10.1038/s41598-019-43148-z

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

© The Author(s) 2019

Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Long non-coding RNA UCA1 was able to bind to UPF1. (A) UCA1 expression was detected by real time PCR and normalized to GAPDH expression. (B) Bivariate correlation between UPF1 and UCA1 RNA expression level in 50 HCC tissues. (C) Cells were treated with Actinomycin D for the indicated time and UCA1 RNA level was evaluated by real time PCR. (D) RIP assay illustrated the binding between UCA1 and UPF1. (E) The overexpression of UPF1 decreased the expression of UCA1. UPF1 plasmid was transfected into Huh7 cells. (F) The knockdown of UPF1 in Huh7 cells increased the expression of UCA1.