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ชื่อเรื่อง: | Anti-proliferation and apoptosis induction in epidermoid carcinoma A431 cells by Artonin E |
ผู้แต่ง: | 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 |
วันที่เผยแพร่: | 2017 |
บทคัดย่อ: | 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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