Description:
Background: Ursane triterpenoids could be considered as novel multi-target therapeutic anticancer agents. Salvurmin A and Salvurmin B are novel cytotoxic ursane triterpenoids isolated
from the aerial parts of Salvia urmiensis, an endemic plant species of Iran.
Methods: In this study, we assessed cytotoxicity of these compounds against two human cancer
cell lines and one human normal cell line and investigated its mechanism via apoptosis and cell
cycle arrest.
Results: Salvurmin A and B showed the most cytotoxic effect on A549 cells compared to other
studied cancer cells. IC50 values for Salvurmin A and B against A549 cells were 35.6 ± 1.5 and
19.2 ± 0.8 µM, respectively. Based on annexin V staining, both of these compounds significantly
induced apoptosis in A549 cells. Moreover, these two compounds significantly increased cell
accumulation in G2/M and decreased the number of cells in G0/G1 phases in A549 cells in a
dose-dependent manner.
Conclusion: Based on the results Salvurmin B can be considered as potential candidate for
further studies against human lung carcinoma.
URL:
http://103.158.96.210:88/web_repository/uploads/no_data.jpg
Type:
Journal
Document:
Diploma III Farmasi
Date:
23-06-2024
Author:
Shima Hashemi