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Betulinic acid modulates the expression of hspa and activates apoptosis in two cell lines of human colorectal cancer

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dc.contributor.author Yurasakpong L.
dc.contributor.author Nantasenamat C.
dc.contributor.author Nobsathian S.
dc.contributor.author Chaithirayanon K.
dc.contributor.author Apisawetakan S.
dc.date.accessioned 2022-03-10T13:17:29Z
dc.date.available 2022-03-10T13:17:29Z
dc.date.issued 2021
dc.identifier.issn 14203049
dc.identifier.other 2-s2.0-85117570002
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/17553
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85117570002&doi=10.3390%2fmolecules26216377&partnerID=40&md5=b726d863583c9e7689085fd413533be0
dc.description.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.
dc.language en
dc.subject antineoplastic agent
dc.subject betulic acid
dc.subject heat shock protein 70
dc.subject pentacyclic triterpene
dc.subject apoptosis
dc.subject cell proliferation
dc.subject cell survival
dc.subject chemistry
dc.subject colorectal tumor
dc.subject conformation
dc.subject dose response
dc.subject drug effect
dc.subject flow cytometry
dc.subject gene expression regulation
dc.subject genetics
dc.subject human
dc.subject metabolism
dc.subject molecular docking
dc.subject molecular dynamics
dc.subject structure activity relation
dc.subject tumor cell line
dc.subject Antineoplastic Agents, Phytogenic
dc.subject Apoptosis
dc.subject Cell Line, Tumor
dc.subject Cell Proliferation
dc.subject Cell Survival
dc.subject Colorectal Neoplasms
dc.subject Dose-Response Relationship, Drug
dc.subject Flow Cytometry
dc.subject Gene Expression Regulation, Neoplastic
dc.subject HSP70 Heat-Shock Proteins
dc.subject Humans
dc.subject Molecular Conformation
dc.subject Molecular Docking Simulation
dc.subject Molecular Dynamics Simulation
dc.subject Pentacyclic Triterpenes
dc.subject Structure-Activity Relationship
dc.title Betulinic acid modulates the expression of hspa and activates apoptosis in two cell lines of human colorectal cancer
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Molecules. Vol 26, No.21 (2021)
dc.identifier.doi 10.3390/molecules26216377


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