Identification of cancer inhibitors from Hystrix brachyura bezoar extracts using LC-MS multivariate data analysis and in silico evaluation on Bcl-2, cyclin B/CDK1, VEGF and NM23-H1; [Identificación de inhibidores de cáncer a partir de extractos de bezoar de Hystrix branchyura usando análisis multivariado LC-MS y evaluación in silico en Bcl-2, cyclin B/CDK1, VEGF, y NM23-H1]

Hystrix brachyura bezoar is calcified undigested material found in the gastrointestinal tract known for various medicinal benefits including as an anticancer agent. However, the H. brachyura population has been declining due to its demand and is under Malaysian law protection. Therefore, present stu...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Boletin Latinoamericano y del Caribe de Plantas Medicinales y Aromaticas
المؤلف الرئيسي: 2-s2.0-85175322681
التنسيق: مقال
اللغة:English
منشور في: MS-Editions 2024
الوصول للمادة أونلاين:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85175322681&doi=10.37360%2fblacpma.24.23.1.4&partnerID=40&md5=fb1c3b2f5b8b5254ecba68132dab1186
الوصف
الملخص:Hystrix brachyura bezoar is calcified undigested material found in the gastrointestinal tract known for various medicinal benefits including as an anticancer agent. However, the H. brachyura population has been declining due to its demand and is under Malaysian law protection. Therefore, present study aimed to identify bezoar anticancer active compounds through metabolomics and in-silico approaches. Five replicates of bezoar powder were subjected to extraction using different solvent ratios of methanol-water (100, 75, 50, 25, 0% v/v). Cytotoxicity and metabolite profiling using liquid chromatography-mass spectrometry were conducted. Putative compounds identified were subjected to in-silico analysis with targeted anticancer proteins namely, Bcl-2, Cyclin B/CDK1 complex, VEGF and NM23-H1. The correlation of LC-MS and cytotoxicity profile pinpointed two compounds, mangiferin and propafenone. In-silico study showed both compounds exerted good binding scores to all proteins with hydrophobic interaction dominating the ligand-protein complex binding, suggesting the ligands act as hydrophobes in the interactions. © 2024, MS-Editions. All rights reserved.
تدمد:7177917
DOI:10.37360/blacpma.24.23.1.4