Reduced ER–mitochondria connectivity promotes neuroblastoma multidrug resistance

Jorida Çoku, David M. Booth, Jan Skoda, Madison C. Pedrotty, Jennifer Vogel, Kangning Liu, Annette Vu, Erica L. Carpenter, Jamie C. Ye, Michelle A. Chen, Peter Dunbar, Elizabeth Scadden, Taekyung D. Yun, Eiko Nakamaru-Ogiso, Estela Area-Gomez, Yimei Li, Kelly C. Goldsmith, C. Patrick Reynolds, Gyorgy Hajnoczky, Michael D. Hogarty

Research output: Contribution to journalArticlepeer-review

Abstract

Most cancer deaths result from progression of therapy resistant disease, yet our understanding of this phenotype is limited. Cancer therapies generate stress signals that act upon mitochondria to initiate apoptosis. Mitochondria isolated from neuroblastoma cells were exposed to tBid or Bim, death effectors activated by therapeutic stress. Multidrug-resistant tumor cells obtained from children at relapse had markedly attenuated Bak and Bax oligomerization and cytochrome c release (surrogates for apoptotic commitment) in comparison with patient-matched tumor cells obtained at diagnosis. Electron microscopy identified reduced ER–mitochondria-associated membranes (MAMs; ER–mitochondria contacts, ERMCs) in therapy-resistant cells, and genetically or biochemically reducing MAMs in therapy-sensitive tumors phenocopied resistance. MAMs serve as platforms to transfer Ca2+ and bioactive lipids to mitochondria. Reduced Ca2+ transfer was found in some but not all resistant cells, and inhibiting transfer did not attenuate apoptotic signaling. In contrast, reduced ceramide synthesis and transfer was common to resistant cells and its inhibition induced stress resistance. We identify ER–mitochondria-associated membranes as physiologic regulators of apoptosis via ceramide transfer and uncover a previously unrecognized mechanism for cancer multidrug resistance.

Original languageEnglish (US)
Article numbere108272
JournalEMBO Journal
Volume41
Issue number8
DOIs
StatePublished - Apr 19 2022

Keywords

  • ceramides
  • inter-organelle contacts
  • mitochondria-associated membranes
  • multidrug resistance
  • sphingolipids

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology
  • Molecular Biology
  • General Neuroscience

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