Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13192
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dc.contributor.authorInnajak S.
dc.contributor.authorTangchirakhaphan S.
dc.contributor.authorNilwarangoon S.
dc.contributor.authorTanjapatkul N.
dc.contributor.authorMahabusarakam W.
dc.contributor.authorWatanapokasin R.
dc.date.accessioned2021-04-05T03:22:41Z-
dc.date.available2021-04-05T03:22:41Z-
dc.date.issued2017
dc.identifier.issn1252208
dc.identifier.other2-s2.0-85075028775
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13192-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85075028775&partnerID=40&md5=bfea5a7eb8b491c45e4bde5fa0ebfbea
dc.description.abstractBackground: Skin cancer is the type of cancer that is becoming an increasingly important public health problem worldwide. The treatment for skin cancer depends on the stage and location of cancer cells. Therefore, the new finding of anti-cancer compound as a therapeutic candidate for skin cancer is necessary. Objective: To investigate the effect of artonin E on anti-proliferation and apoptosis induction in skin cancer epidermoid carcinoma A431 cells. Material and Method: Cell viability and cell proliferation were determined by MTT assay. Nuclear morphological changes, mitochondrial membrane potential and protein expression were determined by Hoechst 33342 and JC-1 staining, respectively. Protein expression was determined by Western blot analysis. Results: Artonin E showed anti-proliferation in A431 treated cells in a dose-dependent manner with an IC50 value of 9.05+6.15 μg/ml. In addition, artonin E induced chromatin condensation and apoptotic bodies in A431 treated cells. JC-1 staining showed that artonin E induced loss of mitochondrial membrane potential. Western blot analysis showed the upregulation of cleaved-caspaase-7 and cleaved-PARP in A431 treated cells. Conclusion: In this study, artonin E showed anti-proliferation and apoptosis induction in A431 treated cells. Moreover, artonin E induced cleaved caspase-7 and cleaved-PARP activation in A431 cells, resulting in apoptosis cell death. Our results indicated that artonin E may be further developed as an anti-cancer drug and the underlying mechanisms of apoptosis induction in A431 cells should be studied. © 2017 Medical Association of Thailand. All rights reserved.
dc.subjectartonin e
dc.subjectcaspase 7
dc.subjectflavonoid
dc.subjectnicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
dc.subjectunclassified drug
dc.subjectA-431 cell line
dc.subjectanti proliferation activity
dc.subjectantineoplastic activity
dc.subjectapoptosis
dc.subjectArticle
dc.subjectcell proliferation
dc.subjectcell proliferation assay
dc.subjectcell structure
dc.subjectcell viability
dc.subjectcell viability assay
dc.subjectchromatin condensation
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdrug activity
dc.subjectfluorescence microscopy
dc.subjecthuman
dc.subjecthuman cell
dc.subjectIC50
dc.subjectmitochondrial membrane potential
dc.subjectMTT assay
dc.subjectproapoptotic activity
dc.subjectprotein expression
dc.subjectskin cancer
dc.subjectsquamous cell carcinoma
dc.subjectupregulation
dc.subjectWestern blotting
dc.titleAnti-proliferation and apoptosis induction in epidermoid carcinoma A431 cells by Artonin E
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationJournal of the Medical Association of Thailand. Vol 100, No.10 (2017), p.S54-S60
Appears in Collections:Scopus 1983-2021

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