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

. 2021 Jan 5;13:13413–13424. doi: 10.2147/OTT.S250377

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

© 2020 Hu 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

LINC00511 knockdown inhibits the malignant phenotypes of CRC. (A) The knockdown efficiency of LINC00511 in HT-29 and HCT8 cells was examined by RT-qPCR. (B) The number of spheroids was determined by performing sphere formation assay. (C) Western blot assay was adopted to determine the levels of proteins (Sox-2, Oct-4, CD44 and Nanog) associated with stemness. (D–E) CCK-8 and colony formation assays were separately used to detect cell viability and proliferation. (F–G) Cell migration and invasion abilities were ensured by transwell assays. *P<0.05, **P<0.01.