Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13192
Title: Anti-proliferation and apoptosis induction in epidermoid carcinoma A431 cells by Artonin E
Authors: Innajak S.
Tangchirakhaphan S.
Nilwarangoon S.
Tanjapatkul N.
Mahabusarakam W.
Watanapokasin R.
Keywords: artonin e
caspase 7
flavonoid
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase
unclassified drug
A-431 cell line
anti proliferation activity
antineoplastic activity
apoptosis
Article
cell proliferation
cell proliferation assay
cell structure
cell viability
cell viability assay
chromatin condensation
controlled study
cytotoxicity
drug activity
fluorescence microscopy
human
human cell
IC50
mitochondrial membrane potential
MTT assay
proapoptotic activity
protein expression
skin cancer
squamous cell carcinoma
upregulation
Western blotting
Issue Date: 2017
Abstract: Background: 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.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13192
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075028775&partnerID=40&md5=bfea5a7eb8b491c45e4bde5fa0ebfbea
ISSN: 1252208
Appears in Collections:Scopus 1983-2021

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