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NRL and CRX Define Photoreceptor Identity and Reveal Subgroup-Specific Dependencies in Medulloblastoma

  • Alexandra Garancher
  • , Charles Y. Lin
  • , Morgane Morabito
  • , Wilfrid Richer
  • , Nathalie Rocques
  • , Magalie Larcher
  • , Laure Bihannic
  • , Kyle Smith
  • , Catherine Miquel
  • , Sophie Leboucher
  • , Nirmitha I. Herath
  • , Fanny Dupuy
  • , Pascale Varlet
  • , Christine Haberler
  • , Christine Walczak
  • , Nadine El Tayara
  • , Andreas Volk
  • , Stéphanie Puget
  • , François Doz
  • , Olivier Delattre
  • Sabine Druillennec, Olivier Ayrault, Robert J. Wechsler-Reya, Alain Eychène, Franck Bourdeaut, Paul A. Northcott, Celio Pouponnot
  • Laboratoire 110
  • Institut Curie
  • Université Paris-Saclay
  • Université Paris-Saclay
  • Université PSL
  • Department of Molecular and Human Genetics
  • Baylor College of Medicine
  • Inserm U830
  • Translational Research in Pediatric Oncology
  • Department of Developmental Neurobiology
  • Department of Immunology
  • Departement de Neuropathologie
  • Centre Hospitalier Sainte-Anne
  • Paris Descartes University
  • McGill University
  • Institute of Neurology
  • Medical University of Vienna
  • INSERM U869
  • AP-HP
  • Hôpital Necker-Enfants Malades
  • SIREDO Center (Care
  • Tumor Initiation & Maintenance Program
  • Sanford Burnham Prebys Medical Discovery Institute

Research output: Contribution to journalArticlepeer-review

56 Citations (Scopus)

Abstract

Cancer cells often express differentiation programs unrelated to their tissue of origin, although the contribution of these aberrant phenotypes to malignancy is poorly understood. An aggressive subgroup of medulloblastoma, a malignant pediatric brain tumor of the cerebellum, expresses a photoreceptor differentiation program normally expressed in the retina. We establish that two photoreceptor-specific transcription factors, NRL and CRX, are master regulators of this program and are required for tumor maintenance in this subgroup. Beyond photoreceptor lineage genes, we identify BCL-XL as a key transcriptional target of NRL and provide evidence substantiating anti-BCL therapy as a rational treatment opportunity for select MB patients. Our results highlight the utility of studying aberrant differentiation programs in cancer and their potential as selective therapeutic vulnerabilities. Garancher et al. show that NRL and CRX are master transcriptional regulators of a photoreceptor-specific differentiation program critical for group 3 medulloblastoma (MB) maintenance. They identify BCL-XL as a key NRL target and provide evidence supporting anti-BCL therapy as a strategy for some MB patients.

Original languageEnglish
Pages (from-to)435-449.e6
JournalCancer Cell
Volume33
Issue number3
DOIs
Publication statusPublished - 12 Mar 2018
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • BCL2
  • CRX
  • MAF
  • NRL
  • apoptosis
  • medulloblastoma
  • photoreceptor
  • retina

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