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DC Field | Value | Language |
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dc.contributor.author | Sirikwan Sangboonruang | en_US |
dc.contributor.author | Kuntida Kitidee | en_US |
dc.contributor.author | Panuwan Chantawannakul | en_US |
dc.contributor.author | Khajornsak Tragoolpua | en_US |
dc.contributor.author | Yingmanee Tragoolpua | en_US |
dc.date.accessioned | 2020-10-14T08:25:27Z | - |
dc.date.available | 2020-10-14T08:25:27Z | - |
dc.date.issued | 2020-08-01 | en_US |
dc.identifier.issn | 20796382 | en_US |
dc.identifier.other | 2-s2.0-85089654342 | en_US |
dc.identifier.other | 10.3390/antibiotics9080517 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089654342&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/70196 | - |
dc.description.abstract | © 2020 by the authors. Licensee MDPI, Basel, Switzerland. Melittin, a major component found in bee venom, is produced by the Apis species of the honey bee. In this study, the effect of melittin derived from Apis florea (Mel-AF), which is a wild honey bee species that is indigenous to Thailand, was investigated against human malignant melanoma (A375) cells. In this study, Mel-AF exhibited considerable potential in the anti-proliferative action of A375 cells. Subsequently, the cellular mechanism of Mel-AF that induced cell death was investigated in terms of apoptosis. As a result, gene and protein expression levels, which indicated the activation of cytochrome-c release and caspase-9 expression, eventually triggered the release of the caspase-3 executioner upon Mel-AF. We then determined that apoptosis-mediated cell death was carried out through the intrinsic mitochondrial pathway. Moreover, advanced abilities, including cell motility and invasion, were significantly suppressed. Mel-AF manipulated the actin arrangement via the trapping of stress fibers that were found underneath the membrane, which resulted in the defective actin cytoskeleton organization. Consequently, the expression of EGFR, a binding protein to F-actin, was also found to be suppressed. This outcome strongly supports the effects of Mel-AF in the inhibition of progressive malignant activity through the disruption of actin cytoskeleton-EGFR interaction and the EGFR signaling system. Thus, the findings of our current study indicate the potential usefulness of Mel-AF in cancer treatments as an apoptosis inducer and a potential actin-targeting agent. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Immunology and Microbiology | en_US |
dc.subject | Medicine | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Melittin from apis florea venom as a promising anticancer agent | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Antibiotics | en_US |
article.volume | 9 | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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