Anthocyanins from Vitis coignetiae Pulliat inhibit cancer invasion and epithelial-mesenchymal transition, but these effects can be attenuated by tumor necrosis factor in human uterine cervical cancer hela cells

24Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Recently we have demonstrated that anthocyanins from fruits of Vitis coignetiae Pulliat (AIMs) have anticancer effects. Here, we investigate the effects of AIMs on cell proliferation and invasion as well as epithelial-mesenchymal transition (EMT) which have been linked to cancer metastasis in human uterine cervical cancer HeLa cells. AIMs inhibited the invasion of HeLa cells in a dose-dependent manner. AIMs inhibited MMP-9 expression in a dose-dependent manner. AIMs inhibited the motility of HeLa cells in a wound healing test. AIMs still suppressed NF-B activation induced by TNF. AIMs also inhibited EMT in HeLa cells. AIMs suppressed vimentin, N-cadherin, and β-catenin expression and induced E-cadherin. AIMs also suppressed expression of β-catenin and Snail, which was regulated by GSK-3. These effects of AIMs were also limited in the HeLa cells treated with TNF. In conclusion, this study indicates that AIMs have anticancer effects by suppressing NF-B-regulated genes and EMT, which relates to suppression of IB phosphorylation and GSK-3 activity, respectively. However, the effects of AIMs were attenuated in the TNF-high condition. © 2013 Jing Nan Lu et al.

Cite

CITATION STYLE

APA

Lu, J. N., Lee, W. S., Yun, J. W., Kim, M. J., Kim, H. J., Kim, D. C., … Shin, S. C. (2013). Anthocyanins from Vitis coignetiae Pulliat inhibit cancer invasion and epithelial-mesenchymal transition, but these effects can be attenuated by tumor necrosis factor in human uterine cervical cancer hela cells. Evidence-Based Complementary and Alternative Medicine, 2013. https://doi.org/10.1155/2013/503043

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free