Nedd4 ubiquitylates VDAC2/3 to suppress erastin-induced ferroptosis in melanoma.
Ferroptosis is a newly defined form of regulated cell death characterized by the iron-dependent accumulation of lipid hydroperoxides. Erastin, the ferroptosis activator, binds to voltage-dependent anion channels VDAC2 and VDCA3, but treatment with erastin can result in the degradation of the channels. Here, the authors show that Nedd4 is induced ... following erastin treatment, which leads to the ubiquitination and subsequent degradation of the channels. Depletion of Nedd4 limits the protein degradation of VDAC2/3, which increases the sensitivity of cancer cells to erastin. By understanding the molecular mechanism of erastin-induced cellular resistance, we can discover how cells adapt to new molecules to maintain homeostasis. Furthermore, erastin-induced resistance mediated by FOXM1-Nedd4-VDAC2/3 negative feedback loop provides an initial framework for creating avenues to overcome the drug resistance of ferroptosis activators.
Mesh Terms:
Animals, Antineoplastic Agents, Cell Line, Tumor, Drug Resistance, Neoplasm, Female, Ferroptosis, Forkhead Box Protein M1, Humans, Melanoma, Mice, Nude, Mitochondrial Membrane Transport Proteins, Nedd4 Ubiquitin Protein Ligases, Piperazines, Ubiquitination, Voltage-Dependent Anion Channel 2, Voltage-Dependent Anion Channels, Xenograft Model Antitumor Assays
Animals, Antineoplastic Agents, Cell Line, Tumor, Drug Resistance, Neoplasm, Female, Ferroptosis, Forkhead Box Protein M1, Humans, Melanoma, Mice, Nude, Mitochondrial Membrane Transport Proteins, Nedd4 Ubiquitin Protein Ligases, Piperazines, Ubiquitination, Voltage-Dependent Anion Channel 2, Voltage-Dependent Anion Channels, Xenograft Model Antitumor Assays
Nat Commun
Date: Dec. 23, 2019
PubMed ID: 31974380
View in: Pubmed Google Scholar
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