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 Apr 30;13:3641–3652. doi: 10.2147/OTT.S237576

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

© 2020 Wang 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

NNT-AS1 was a sponge of miR-1236-3p. (A) Predictive binding sites between NNT-AS1 and miR-1236-3p. (B and C) Dual-luciferase reporter analysis for the luciferase activities of WT-NNT-AS1 and MUT-NNT-AS1 in DDP-resistant cells was detected. (D) Relative level of miR-1236-3p in lung cancer tissues compared with adjacent normal tissues. (E) The correlation between miR-1236-3p level and NNT-AS1 level. (F and G) QRT-PCR analysis for the level of miR-1236-3p in (F) lung cancer cells and (G) DDP-resistant cells was detected. (H) The level of miR-1236-3p after transfection with NNT-AS1 in vitro. (I and J) QRT-PCR analysis for the impact of NNT-AS1 overexpression or detection on the level of miR-1236-3p in A549/DDP and H522/DDP cells were measured. *P<0.05.