Nature Communications (Jun 2022)

Persister state-directed transitioning and vulnerability in melanoma

  • Heike Chauvistré,
  • Batool Shannan,
  • Sheena M. Daignault-Mill,
  • Robert J. Ju,
  • Daniel Picard,
  • Stefanie Egetemaier,
  • Renáta Váraljai,
  • Christine S. Gibhardt,
  • Antonio Sechi,
  • Farnusch Kaschani,
  • Oliver Keminer,
  • Samantha J. Stehbens,
  • Qin Liu,
  • Xiangfan Yin,
  • Kirujan Jeyakumar,
  • Felix C. E. Vogel,
  • Clemens Krepler,
  • Vito W. Rebecca,
  • Linda Kubat,
  • Smiths S. Lueong,
  • Jan Forster,
  • Susanne Horn,
  • Marc Remke,
  • Michael Ehrmann,
  • Annette Paschen,
  • Jürgen C. Becker,
  • Iris Helfrich,
  • Daniel Rauh,
  • Markus Kaiser,
  • Sheraz Gul,
  • Meenhard Herlyn,
  • Ivan Bogeski,
  • José Neptuno Rodríguez-López,
  • Nikolas K. Haass,
  • Dirk Schadendorf,
  • Alexander Roesch

DOI
https://doi.org/10.1038/s41467-022-30641-9
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 17

Abstract

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Slow-cycling melanoma persister cells are characterised by a high, reversible expression of H3K4 demethylase KDM5B. Here, the authors use genetic and chemical methods to enforce a permanent high expression of KDM5B and show that these cells transit to a melanocytic differentiated state and undergo cell cycle arrest.