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Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells

  • Authors:
    • Sang Gyu Lee
    • Dong Gun Lee
    • Yong Hoon Joo
    • Namhyun Chung
  • View Affiliations / Copyright

    Affiliations: Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea, Department of Biosystems and Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea
    Copyright: © Lee et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 667
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    Published online on: July 14, 2021
       https://doi.org/10.3892/ol.2021.12928
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Abstract

Various therapies have been developed to target malignant melanoma, which is associated with a high mortality rate worldwide. Although dacarbazine (DTIC) is employed for treating melanoma, it is associated with several side effects. Hence, patients with melanoma are co‑treated with additional drugs to mitigate the side effects of DTIC. In the present study, synergistic therapeutic effects of the DTIC/oxyresveratrol (ORT) combination were examined using the human malignant melanoma WM‑266‑4 cell line. Treatment with ORT and DTIC inhibited the proliferation of WM‑266‑4 cells. Compared with those in the ORT‑ and DTIC‑treated groups, the proportion of cells arrested at the S phase, as well as apoptotic rates, were increased in the ORT and DTIC co‑treatment group. In WM‑266‑4 cells, synergistic proliferation‑inhibitory activities of the ORT/DTIC combination were assessed based on cell viability and migration, antioxidant capacity, cytokine production, cell cycle arrest, apoptotic rate and protein expression through WST‑1 assay, wound healing assay, flow cytometry and western blotting. Furthermore, the expression levels of proteins, including NOTCH, involved in the pathogenesis of solid cancers, such as melanoma, were examined. Overall, the ORT/DTIC combination synergistically promoted cell cycle arrest at the S phase and the apoptosis of WM‑266‑4 cells. Thus, this combination treatment may serve as a novel therapeutic strategy for treating malignant melanoma.
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Copy and paste a formatted citation
Spandidos Publications style
Lee SG, Lee DG, Joo YH and Chung N: Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells. Oncol Lett 22: 667, 2021.
APA
Lee, S.G., Lee, D.G., Joo, Y.H., & Chung, N. (2021). Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells. Oncology Letters, 22, 667. https://doi.org/10.3892/ol.2021.12928
MLA
Lee, S. G., Lee, D. G., Joo, Y. H., Chung, N."Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells". Oncology Letters 22.3 (2021): 667.
Chicago
Lee, S. G., Lee, D. G., Joo, Y. H., Chung, N."Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells". Oncology Letters 22, no. 3 (2021): 667. https://doi.org/10.3892/ol.2021.12928
Copy and paste a formatted citation
x
Spandidos Publications style
Lee SG, Lee DG, Joo YH and Chung N: Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells. Oncol Lett 22: 667, 2021.
APA
Lee, S.G., Lee, D.G., Joo, Y.H., & Chung, N. (2021). Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells. Oncology Letters, 22, 667. https://doi.org/10.3892/ol.2021.12928
MLA
Lee, S. G., Lee, D. G., Joo, Y. H., Chung, N."Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells". Oncology Letters 22.3 (2021): 667.
Chicago
Lee, S. G., Lee, D. G., Joo, Y. H., Chung, N."Synergistic inhibitory effects of the oxyresveratrol and dacarbazine combination against melanoma cells". Oncology Letters 22, no. 3 (2021): 667. https://doi.org/10.3892/ol.2021.12928
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