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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Screening of Anti-Cancer Properties of Beta-Sitosterol and its Derivatives against Microtubules: Molecular Modeling Approach

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Author(s):
Karthik, Lakshminarayanan [1] ; Vijayakumar, Balakrishnan [2]
Total Authors: 2
Affiliation:
[1] Meenakshi Acad Higher Educ & Res, Cent Res Lab, Chennai 600078, Tamil Nadu - India
[2] Univ Sao Paulo, Sao Carlos Inst Phys IFSC, Av Joao Dagnone 1100, BR-13563120 Sao Carlos, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND PHYTOPHARMACOLOGICAL RESEARCH; v. 10, n. 1, p. 8+, 2020.
Web of Science Citations: 0
Abstract

A phytosterol compound, beta-sitosterol is found in abundance in many plants, s, and vegetables. They possess numerous health benefits and clinical uses including medicinal properties such as anti-diabetic, antiatherogenic, anti-asthmatic, etc. The compound was also reported to possess anti-cancer property against various cancer cell lines. Microtubules which are hollow fibrous shafts and made up of tubulin protein play essential roles in cell division, cell movement and intracellular transport. Due to their major role in cell division, microtubules are considered as an attractive target for designing potent anti-cancer agents. Given their importance, the present study describes the molecular docking of beta-sitosterol and its analogs with the alpha/beta form of tubulin. For this, small molecule compounds structurally similar to beta-sitosterol were retrieved from PubChem and Binding database. In the subsequent step, High Throughput Virtual screening was carried out with the tuhulin-colchicine complex. Based on the virtual screening results and the nature of active site residues of the protein complex, the screened compounds were further taken to Induced Fit Docking studies using Schrodinger's GLIDE. Hydrogen bond interactions were analyzed between the compounds and active site amino acid residues. QikProp module and FAF-Drugs tools were used to analyze the pharmacokinetic properties of the selected compounds. Among the tested compounds, few compounds were found to satisfy all the in silico parameters and can be developed as potent inhibitors targeting microtubules. (AU)

FAPESP's process: 18/00492-4 - Determination of the molecular structure of the human pyruvate carrier subunit 2, MPC2
Grantee:Vijayakumar Balakrishnan
Support Opportunities: Scholarships in Brazil - Post-Doctoral