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Article

Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway

  • Authors:
    • Zheng Li
    • Xiao Liu
    • Ming Li
    • Jingxiu Chai
    • Shan He
    • Jinfeng Wu
    • Jinhua Xu
  • View Affiliations / Copyright

    Affiliations: Department of Dermatology, Huashan Hospital, Fudan University, Shanghai 200040, P.R. China
  • Pages: 566-574
    |
    Published online on: April 28, 2020
       https://doi.org/10.3892/mmr.2020.11095
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Abstract

BRAF inhibitors are some of the most effective drugs against melanoma; however, their clinical application is largely limited by drug resistance. Juglone, isolated from walnut trees, has demonstrated anti‑tumour activity. In the present study, it was investigated whether juglone could enhance the responses to a BRAF inhibitor in melanoma cells (A375R and SK‑MEL‑5R) with an acquired resistance. These cells were treated with juglone alone, BRAF inhibitor (PLX4032) alone, or juglone combined with PLX4032. It was demonstrated that the combination of juglone and PLX4032 had synergistic effects on BRAF inhibitor‑resistant melanoma cells. Juglone potentiated PLX4032‑induced cytotoxicity and mitochondrial apoptosis in both A375R and SK‑MEL‑5R cells, which was accompanied by a decline in mitochondrial membrane potential and a decrease in Bcl‑2/Bax ratio. Moreover, juglone combined with PLX4032 markedly increased the intracellular level of reactive oxygen species (ROS) and activated p38 and p53, as compared with juglone alone or PLX4032 alone. Pre‑treatment with N‑acetyl‑L‑cysteine, a ROS scavenger, completely reversed the cytotoxicity induced by juglone combined with PLX4032. In conclusion, juglone potentiated BRAF inhibitor‑induced apoptosis in resistant melanoma cells, and these effects occurred partially through ROS and the p38‑p53 pathway, suggesting the potential of juglone as a sensitizer to BRAF inhibitors in the treatment of melanoma.
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Copy and paste a formatted citation
Spandidos Publications style
Li Z, Liu X, Li M, Chai J, He S, Wu J and Xu J: Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway. Mol Med Rep 22: 566-574, 2020.
APA
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., & Xu, J. (2020). Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway. Molecular Medicine Reports, 22, 566-574. https://doi.org/10.3892/mmr.2020.11095
MLA
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., Xu, J."Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway". Molecular Medicine Reports 22.1 (2020): 566-574.
Chicago
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., Xu, J."Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway". Molecular Medicine Reports 22, no. 1 (2020): 566-574. https://doi.org/10.3892/mmr.2020.11095
Copy and paste a formatted citation
x
Spandidos Publications style
Li Z, Liu X, Li M, Chai J, He S, Wu J and Xu J: Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway. Mol Med Rep 22: 566-574, 2020.
APA
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., & Xu, J. (2020). Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway. Molecular Medicine Reports, 22, 566-574. https://doi.org/10.3892/mmr.2020.11095
MLA
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., Xu, J."Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway". Molecular Medicine Reports 22.1 (2020): 566-574.
Chicago
Li, Z., Liu, X., Li, M., Chai, J., He, S., Wu, J., Xu, J."Juglone potentiates BRAF inhibitor‑induced apoptosis in melanoma through reactive oxygen species and the p38‑p53 pathway". Molecular Medicine Reports 22, no. 1 (2020): 566-574. https://doi.org/10.3892/mmr.2020.11095
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