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 12;12:3343–3352. doi: 10.2147/CMAR.S250772

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

© 2020 Lin et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

PMC Copyright notice

C-MET is a direct downstream target of miR-340. (A) Schematic of the construction of wild-type or mutant c-MET 3ʹ-UTR vectors is illustrated. (B) Relative luciferase activity was analyzed in U251 and LN229 cells. Firefly luciferase vector was used as an internal control. (C) Western blot results of c-MET protein in U251 and LN229 cells transduced with miR-340 and negative control. (D) The representative IHC pictures showed the c-MET protein expression in tissue with high or low miR-340 expression. (E) The relative expression level of c-MET by IHC in groups with high or low miR-340. **P<0.01.