Back to Search Start Over

Arctigenin Induces Apoptosis in Melanoma Cells by Reducing the Expression of BCL-2 and VEGF.

Authors :
Gao, Yang
Wang, He-peng
Wang, Hai-fei
Ma, Shi-meng
Du, Zi-wei
Liu, Jia
Source :
Transplantation Proceedings. Mar2024, Vol. 56 Issue 2, p448-452. 5p.
Publication Year :
2024

Abstract

To investigate the biological effects of arctigenin on B16-F10 melanoma cells in vitro and to explore its mechanism. B16-F10 melanoma cells in vitro were treated with the blank control solution and arctigenin solution of different concentrations, respectively. Cell proliferation and apoptosis were analyzed using the CCK-8 assay and cell loss assay, and the effect of arctigenin on melanoma cell proliferation was evaluated. Western blot was used to analyze the expression of BCL-2 protein and vascular endothelial growth factor (VEGF) in the cells of different groups and to explore the mechanism of action of arctigenin. The proliferation rate of B16-F10 melanoma cells treated with arctigenin solutions was significantly lower than that of the blank control group (P <.05), and the proliferation rate decreased with increasing concentration of arctigenin. The apoptosis rate of B16-F10 melanoma cells treated with arctigenin solutions was significantly higher than that of the blank control group (P <.05), and the apoptosis rate increased with increasing concentration of arctigenin. The expression levels of BCL-2 and VEGF in B16-F10 melanoma cells treated with arctigenin solutions were significantly lower than those in the blank control group (P <.05), and the expression levels decreased as the concentration of arctigenin increased. Arctigenin can inhibit the proliferation and promote the apoptosis of melanoma cells, and the mechanism may be associated with decreasing the expression of BCL-2 and VEGF in melanoma cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00411345
Volume :
56
Issue :
2
Database :
Academic Search Index
Journal :
Transplantation Proceedings
Publication Type :
Academic Journal
Accession number :
175982480
Full Text :
https://doi.org/10.1016/j.transproceed.2024.01.054