Abstract
Targeting the apoptosis-inducing pathway has drawn much attention in searching for a novel anticancer drug. Bcl-2 is the most studied antiapoptotic protein, recognised in aiding in cell survival and overexpressed in most cancer cells resulting in cancer resistance toward conventional treatment. The inhibition of Bcl-2 proteins become the main target for inducing apoptosis in cancer cells. β-mangostin received minimum attention in investigating anticancer properties as compared to its family such αmangostin. We performed molecular docking of β-mangostin, doxorubicin (in silico control) and ABT-737 (co-crystal Bcl-2 inhibitor) against antiapoptotic Bcl-2 protein using PyMol, Discovery Studio Biovia 2021, AutoDock Vina, and AutoDock Tools version 1.5.7. The result demonstrates for the first time that β-mangostin showed an optimum binding affinity with Bcl-2 (∆G −7.3 kcal/mol), similar to those shown by doxorubicin. The present results indicate that β-mangostin could potentially serve as Bcl-2 protein inhibitors, which would consequently lead to an apoptotic process in oral cancers. The present data warrant validation using in vitro and in vivo assays.
Metadata
Item Type: | Article |
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Creators: | Creators Email / ID Num. Abdullah, Mohamad Zakkirun zakkirun@iium.edu.my Bakar, Latifah Munirah UNSPECIFIED Arief Ichwan, Solachuddin Jauhari UNSPECIFIED Othman, Noratikah UNSPECIFIED Taher, Muhammad UNSPECIFIED |
Subjects: | R Medicine > RC Internal Medicine > Cancer R Medicine > RC Internal Medicine > Cancer > Research. Experimentation |
Divisions: | Universiti Teknologi MARA, Pulau Pinang > Permatang Pauh Campus |
Journal or Publication Title: | ESTEEM Academic Journal |
UiTM Journal Collections: | UiTM Journal > ESTEEM Academic Journal (EAJ) |
ISSN: | 1675-7939 |
Volume: | 18 |
Page Range: | pp. 128-138 |
Keywords: | Bcl-2, β-mangostin; apoptosis, binding affinity, in silico molecular docking |
Date: | March 2022 |
URI: | https://ir.uitm.edu.my/id/eprint/62610 |