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 27;12:1493–1502. doi: 10.2147/CMAR.S246691

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

© 2020 Shen 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

Curcumin inhibited the viability, colony formation and induced the apoptosis of breast cancer cells. (A) Cell viability of MCF-7 and MDA-MB-231 cells treated by different concentrations of curcumin (0, 10, 20 and 30 μM) for 24 and 48 h was detected by MTT assay; (B) Colony formation rate of MCF-7 and MDA-MB-231 cells treated with different concentrations of curcumin was detected by colony formation assay; (C) Apoptosis rate of MCF-7 and MDA-MB-231 cells treated with different concentrations of curcumin was detected by Flow cytometry. *P < 0.05, **P < 0.01 vs 0 μM.