ANTICANCER ACTIVITY OF Î’-SITOSTEROL FROM PLECTRANTHUS AMBOINICUS (LOUR. SPRENG.) LEAVES: IN VITRO AND IN SILICO STUDIES
Keywords:Nil, Inhibitor, Anticancer, In vitro, In silico
Objective: Î²-sitosterol is the steroid compound which is an important nutrient in the diet meal, hydrophobic and soluble in organic solvents and considered as a good biomarker due to its biological activity.
Methods: In vitro study was using 2,5-diphenyl tetrazolium bromide method towards T47D, MCF-7, HeLa, and WiDr cell lines. In silico docking using PLANTS program and visualized by Yasara program. The model of three dimension enzyme structures used in this research were epidermal growth factor receptor (EGFR), phosphatidylinositol-3-kinase (PI3K), estrogen receptor-alpha (ER-Î±), ER-beta (ER-Î²), and human EGFR 2 (HER-2). Two and three dimensions of Î²-sitosetrol, ZSTK474, and tamoxifen as the standard were generated using Marvin Sketch program.
Results: Î²-sitosterol was found to have inhibitory concentration 50% of 0.55; 0.87; 0.76, and 0.99 mM. Î²-sitosterol and ZSTK474 were inhibited EGFR and PI3K with docking score âˆ’92.8195; âˆ’91.7920 and âˆ’91.7470; âˆ’94.7491 Î²-sitosterol and tamoxifen were inhibited ER-Î±, ER-Î² and HER-2 with docking score âˆ’78.5570; âˆ’89.535, âˆ’68.7717; âˆ’52.008 and âˆ’90.4908; âˆ’50.5576, respectively.
Conclusion: Based on the results above that shows Î²-sitosterol provide effective as anticancer.
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