2018
DOI: 10.3892/ol.2018.9379
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Antitumorigenic effect of damnacanthal on melanoma cell viability through p53 and NF‑κB/caspase‑3 signaling pathways

Abstract: Melanoma is highly malignant, particularly prone to metastasizing to the skin. The incidence of melanoma varies markedly between countries, and is relatively low in China. The aim of the present study was to investigate the antitumorigenic effect of damnacanthal on melanoma cells, and its molecular mechanism. MUM-2B cells were treated with 0-20 µM damnacanthal for 12, 24 and 48 h. In vitro, it was demonstrated that damnacanthal inhibited proliferation and promoted apoptosis of melanoma cells in a dose-and time… Show more

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Cited by 2 publications
(1 citation statement)
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“…IFN-α/β signaling affects the p53 responses in tumor suppression and antiviral defense (43). The sensitization effect of IFN-β in TMZ-treated melanoma cells is dependent on p53 (15), in which p21 is directly activated (44). In addition to growth inhibition, G 2 /M cell cycle arrest as a result of p21 activation following treatment with TMZ plus IFN-β was observed in the present study.…”
Section: Discussionsupporting
confidence: 66%
“…IFN-α/β signaling affects the p53 responses in tumor suppression and antiviral defense (43). The sensitization effect of IFN-β in TMZ-treated melanoma cells is dependent on p53 (15), in which p21 is directly activated (44). In addition to growth inhibition, G 2 /M cell cycle arrest as a result of p21 activation following treatment with TMZ plus IFN-β was observed in the present study.…”
Section: Discussionsupporting
confidence: 66%