Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13144
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dc.contributor.authorTayeh M.
dc.contributor.authorNilwarangkoon S.
dc.contributor.authorTanunyutthawongse C.
dc.contributor.authorMahabusarakum W.
dc.contributor.authorWatanapokasin R.
dc.date.accessioned2021-04-05T03:22:25Z-
dc.date.available2021-04-05T03:22:25Z-
dc.date.issued2018
dc.identifier.issn17920981
dc.identifier.other2-s2.0-85046544304
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13144-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85046544304&doi=10.3892%2fetm.2018.6044&partnerID=40&md5=ef9fbac15237d1daff52d3b2531402bb
dc.description.abstractRhodomyrtone is a bioactive compound extracted from Rhodomyrtus tomentosa leaves. It has been used as a traditional herb medicine for many years. Rhodomyrtone exhibits antibacterial activity, anti-inflammatory and antioxidant activities. However, the anticancer activity of rhodomyrtone has not been previously reported. The present study investigated the anticancer effect of rhomyrtone on human epidermoid carcinoma A431 cells. The cytotoxic and antiproliferative effects of rhodomyrtone on A431 cells were investigated by an MTT assay. Cell morphological alterations and apoptotic cells were observed with Hoechst 33342 staining following rhodomyrtone treatment. Flow cytometry and western blotting were performed to detect cell cycle and apoptosis induction. The results demonstrated that rhodomyrtone inhibited proliferation of A431 cells in a dose-dependent manner with IC50 value of 8.04±0.11 µg/ml. The results also indicated that rhodomyrtone increased chromatin condensation, nuclear fragmentation and apoptotic bodies in treated A431 cells in a time-dependent manner. Apoptosis was also induced through the activation of caspase-7 and poly (ADP-Ribose) polymerase cleavage. Flow cytometry analysis revealed that rhodomyrtone induced cell cycle arrest at the G1 phase. Notably, the non-toxic concentration of rhodomyrtone markedly inhibited A431 cell migration in a dose- and time-dependent manner. These finding suggested that rhodomyrtone may be used as an anticancer agent for human skin cancer. © 2018, Spandidos Publications. All rights reserved.
dc.subjectcaspase 7
dc.subjectnicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
dc.subjectplant medicinal product
dc.subjectrhodomyrtone
dc.subjectunclassified drug
dc.subjectantineoplastic activity
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcell migration
dc.subjectcell proliferation
dc.subjectchromatin condensation
dc.subjectcontrolled study
dc.subjectflow cytometry
dc.subjectfluorescence microscopy
dc.subjectG1 phase cell cycle checkpoint
dc.subjectgrowth inhibition
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC50
dc.subjectMTT assay
dc.subjectskin cancer
dc.subjectWestern blotting
dc.subjectwound healing
dc.titleApoptosis and antimigration induction in human skin cancer cells by rhodomyrtone
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationExperimental and Therapeutic Medicine. Vol 15, No.6 (2018), p.5035-5040
dc.identifier.doi10.3892/etm.2018.6044
Appears in Collections:Scopus 1983-2021

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