Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/17553
Title: Betulinic acid modulates the expression of hspa and activates apoptosis in two cell lines of human colorectal cancer
Authors: Yurasakpong L.
Nantasenamat C.
Nobsathian S.
Chaithirayanon K.
Apisawetakan S.
Keywords: antineoplastic agent
betulic acid
heat shock protein 70
pentacyclic triterpene
apoptosis
cell proliferation
cell survival
chemistry
colorectal tumor
conformation
dose response
drug effect
flow cytometry
gene expression regulation
genetics
human
metabolism
molecular docking
molecular dynamics
structure activity relation
tumor cell line
Antineoplastic Agents, Phytogenic
Apoptosis
Cell Line, Tumor
Cell Proliferation
Cell Survival
Colorectal Neoplasms
Dose-Response Relationship, Drug
Flow Cytometry
Gene Expression Regulation, Neoplastic
HSP70 Heat-Shock Proteins
Humans
Molecular Conformation
Molecular Docking Simulation
Molecular Dynamics Simulation
Pentacyclic Triterpenes
Structure-Activity Relationship
Issue Date: 2021
Abstract: Betulinic acid (BA) is a pentacyclic triterpene usually isolated from botanical sources. Numerous studies have reported the inhibitory effect of BA against human colorectal cancer cells (CRC). However, its effect on the expression of the molecular chaperone HSPA is unclear. The aim of this research is to investigate the anti-cancer activities of BA purified from Piper retrofractum and study its effect on the expression of HSPA in colorectal cancer HCT116 and SW480 cells. The viability of both cancer cells was reduced after they were treated with an increasing dosage of BA. Flow cytometry assay revealed that levels of cell apoptosis significantly increased after incubation with BA in both cancer cells. Pro-apoptotic markers including Bax, cleaved-caspase-3 and cleaved-caspase-9 were increased while anti-apoptotic marker Bcl-2 was decreased after BA treatment. Western blot also showed that the expression of HSPA fluctuated upon BA treatment, whereby HSPA was increased at lower BA concentrations while at higher BA concentrations HSPA expression was decreased. Preliminary molecular docking assay showed that BA can bind to the nucleotide binding domain of the HSP70 at its ADP-bound state of the HSP70. Although further research is needed to comprehend the BA-HSPA interaction, our findings indicate that BA can be considered as potential candidate for the development of new treatment for colorectal cancer. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI: https://ir.swu.ac.th/jspui/handle/123456789/17553
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85117570002&doi=10.3390%2fmolecules26216377&partnerID=40&md5=b726d863583c9e7689085fd413533be0
ISSN: 14203049
Appears in Collections:Scopus 1983-2021

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