Long-term depletion of cereblon induces mitochondrial dysfunction in cancer cells

BMB Rep. 2021 Jun;54(6):305-310. doi: 10.5483/BMBRep.2021.54.6.218.

Abstract

Cereblon (CRBN) is a multi-functional protein that acts as a substrate receptor of the E3 ligase complex and a molecular chaperone. While CRBN is proposed to function in mitochondria, its specific roles are yet to be established. Here, we showed that knockdown of CRBN triggers oxidative stress and calcium overload in mitochondria, leading to disruption of mitochondrial membrane potential. Notably, long-term CRBN depletion using PROteolysis TArgeting Chimera (PROTAC) induced irreversible mitochondrial dysfunction, resulting in cell death. Our collective findings indicate that CRBN is required for mitochondrial homeostasis in cells. [BMB Reports 2021; 54(6): 305-310].

MeSH terms

  • Adaptor Proteins, Signal Transducing / deficiency*
  • Apoptosis
  • Calcium / metabolism
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology*
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology*
  • Membrane Potential, Mitochondrial
  • Mitochondria / metabolism
  • Mitochondria / pathology*
  • Oxidative Stress*
  • Proteasome Endopeptidase Complex / metabolism*
  • Proteolysis*
  • Ubiquitin-Protein Ligases / deficiency*
  • Ubiquitination

Substances

  • Adaptor Proteins, Signal Transducing
  • CRBN protein, human
  • Ubiquitin-Protein Ligases
  • Proteasome Endopeptidase Complex
  • Calcium