4.8 Article

ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry

Journal

NATURE COMMUNICATIONS
Volume 10, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-019-13515-5

Keywords

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Funding

  1. National Cancer Institute, National Institute of Health [K99 CA157951, R01 CA180692]
  2. American Lebanese Syrian Associated Charities (ALSAC)
  3. National Research Foundation (NRF), Prime Minister's Office, Singapore under its Competitive Research Programme [NRF-NRFF2013-02]
  4. Ministry of Education (MOE), Singapore [FRC T1-2015 Sep-07]
  5. NRF
  6. MOE under its Research Centres of Excellence initiative
  7. Damon Runyon Cancer Research Foundation [DRG-24-18, DRSG-9-14]
  8. Alex's Lemonade Stand Foundation
  9. American Society for Clinical Oncology
  10. Rally Foundation for Childhood Cancer Research
  11. Claudia Adams Barr Program for Innovative Cancer Research

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A heritable polymorphism within regulatory sequences of the LMO1 gene is associated with its elevated expression and increased susceptibility to develop neuroblastoma, but the oncogenic pathways downstream of the LMO1 transcriptional co-regulatory protein are unknown. Our ChIP-seq and RNA-seq analyses reveal that a key gene directly regulated by LMO1 and MYCN is ASCL1, which encodes a basic helix-loop-helix transcription factor. Regulatory elements controlling ASCL1 expression are bound by LMO1, MYCN and the transcription factors GATA3, HAND2, PHOX2B, TBX2 and ISL1-all members of the adrenergic (ADRN) neuroblastoma core regulatory circuitry (CRC). ASCL1 is required for neuroblastoma cell growth and arrest of differentiation. ASCL1 and LMO1 directly regulate the expression of CRC genes, indicating that ASCL1 is a member and LMO1 is a coregulator of the ADRN neuroblastoma CRC.

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