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 Feb 19;13:1569–1581. doi: 10.2147/OTT.S237307

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

© 2020 Sun 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

Effects of MAPK1 on the progression of TC cells.

Notes: TPC-1 and HTH83 cells were co-transfected with si-MAPK1 and anti-miR-940. (A) WB analysis was used to assess the protein level of MAPK1 to evaluate the transfection efficiency of si-MAPK1 and anti-miR-940. (B) Colony formation assay was performed to detect the number of colonies in TPC-1 and HTH83 cells. (C and D) Transwell assay was used to measure the number of migrated and invaded TPC-1 and HTH83 cells. (E and F) The OCR of basal respiration and maximum respiration in TPC-1 and HTH83 cells was determined by Seahorse XF Extracellular Flux Analyzer. *P < 0.05.