Effects of Chrysin on Oral Squamous Cell Carcinoma in Vitro

dc.contributor.authorPuengsurin D.
dc.contributor.authorBuranapraditkun S.
dc.contributor.authorLeewansangtong C.
dc.contributor.authorTaechaaukarakul N.
dc.contributor.authorSongsivilai P.
dc.contributor.authorSurarit R.
dc.contributor.authorKitkumthorn N.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T17:06:20Z
dc.date.available2023-06-18T17:06:20Z
dc.date.issued2022-01-01
dc.description.abstractObjective Chrysin is a hydroxylated flavonoid derived from propolis or bee glue, a natural product. Previous research on chrysin's biological functions, including anticancer activity, had been reported. However, chrysin's effect on oral squamous cell carcinoma (OSCC) is still scarce. This article aimed to test the cytotoxicity, antiproliferative, antimigration, anti-invasion, and apoptotic effects of purified chrysin in two OSCC cell lines, HSC4 and SCC25. Materials and Methods The malignant phenotype was assessed using cell proliferation, wound healing, and transwell assays. Cell apoptosis was determined using flow cytometry. The positive control was OSCC cells treated with cisplatin, and the negative control was OSCC cells incubated with 0.1% dimethyl sulfoxide. Results Chrysin at concentrations of 100 and 200 μM could inhibit OSCC cell proliferation, migration, and invasion, as well as enhance cell apoptosis, particularly in the early stages of apoptosis. Conclusion In OSCC cell lines, chrysin has been demonstrated to be an effective antioncogenic agent. Additional research is required to confirm the results. Chrysin should be suggested as a possible alternative therapeutic application for OSCC.
dc.identifier.citationEuropean Journal of Dentistry (2022)
dc.identifier.doi10.1055/s-0042-1755624
dc.identifier.eissn13057464
dc.identifier.issn13057456
dc.identifier.scopus2-s2.0-85139870050
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/84468
dc.rights.holderSCOPUS
dc.subjectDentistry
dc.titleEffects of Chrysin on Oral Squamous Cell Carcinoma in Vitro
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85139870050&origin=inward
oaire.citation.titleEuropean Journal of Dentistry
oairecerif.author.affiliationMahidol University, Faculty of Dentistry
oairecerif.author.affiliationKing Chulalongkorn Memorial Hospital
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University

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