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 May 19;19:92. doi: 10.1186/s12943-020-01213-6

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 — circMET may function as a sponge for miR-30-5p a. The circRIP assay showed a specific enrichment of circMET and miR-30-5p compared with that in the negative control; b. A schematic drawing showing the putative binding sites of wt-miR-30s-5p and mu-miR-30s-5p in circMET; c. The luciferase activity of luc-circMET and mutant luc-circMET in HEK293T cells after cotransfection with miR-30-5p; d. The circRIP assay was performed in HEK293T cells using biotin-labeled miR-30-5p mimics and a negative control (NC); e. FISH analysis in HCCLM3 and Huh7 cells revealed that circMET colocalized with miR-30a-5p in the cytoplasm; f. miR-30a/e-5p knockdown in cells with low levels of circMET upregulated the cell invasive ability. Left, representative pictures of transwell assay. Right, statistic of transwell assay