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

. 2023 Aug 21;42:215. doi: 10.1186/s13046-023-02777-z

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

© The Author(s) 2023

Open Access This 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. 2 — Knockdown of METTL1 inhibits CRPC cell proliferation and invasion. A-B Detection of METTL1 mRNA and protein level between the HSPC and CRPC cell lines. C-E METTL1 knockdown efficiency in LNCaP-AI and C4-2 cells via RT-qPCR and western blot. F-K Validation of proliferation ability change after METTL1 was inhibited in LNCaP-AI and C4-2 cells through MTT (F, G) and colony formation (H-K) assays. L-O Transwell was performed to determine the invasion capacity variation of LNCaP-AI and C4-2 cells caused by METTL1 suppression. Three biological replicates of each experiment were performed. ***P < 0.001; ****P < 0.0001