4.7 Article

Novel potential NOX2 inhibitors, Dudleya brittonii water extract and polygalatenoside A inhibit intracellular ROS generation and growth of melanoma

Journal

BIOMEDICINE & PHARMACOTHERAPY
Volume 150, Issue -, Pages -

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.112967

Keywords

Dudleya brittonii; Polygalatenoside; NADPH oxidase; Antioxidant; Reactive oxygen species; Melanoma

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2021R1F1A1049562]
  2. R&D Program for Forest Science Technology by the Korea Forest Service (Korea Forestry Promotion Institute) [2021374C10-2123-BD02]
  3. Korea Forestry Promotion Institute (KOFPI) [2021374C10-2123-BD02] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2021R1F1A1049562] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Reactive oxygen species (ROS) play a crucial role in regulating the proliferation, metastasis, and drug resistance of melanoma, and the inhibition of NOX2 and cytosolic ROS by Dudleya brittonii water extract (DBWE) and its bioactive substance polygalatenoside A may contribute to the prevention and treatment of melanoma. DBWE also inhibits mitochondrial activity, lipid metabolism, and cell cycle in B16-F10 melanoma cells.
Reactive oxygen species (ROS) are key regulators of the proliferation, metastasis, and drug resistance of mela-noma, which accounts for 60% of skin cancer deaths. In a previous study, we developed Dudleya brittonii water extract (DBWE) with antioxidant activity, but the mechanism of action and bioactive substances of DBWE have not been fully identified. This study showed altered NADPH oxidase 2 (NOX2) expression and selective inhibition of cytosolic ROS but not mitochondrial ROS in B16-F10 melanoma cells, suggesting the NOX2 inhibitory po-tential of DBWE. In addition, DBWE inhibited mitochondrial activity, lipid metabolism, and cell cycle in B16-F10 cells. The anti-melanoma effect of DBWE was abrogated by the addition of ROS, and there was no significant change in the melanogenesis pathway. Polygalatenoside A was identified as a candidate bioactive substance in the DBWE aqueous fraction through mass spectrometry, and the DBWE-like anti-melanoma effect was confirmed. These data suggest that DBWE and polygalatenoside A have the potential to prevent and treat melanoma.

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