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Cancers (Basel). 2021 Dec 10;13(24). doi: 10.3390/cancers13246215.

Increased Replication Stress Determines ATR Inhibitor Sensitivity in Neuroblastoma Cells.

Cancers

David King, Harriet E D Southgate, Saskia Roetschke, Polly Gravells, Leona Fields, Jessica B Watson, Lindi Chen, Devon Chapman, Daniel Harrison, Daniel Yeomanson, Nicola J Curtin, Deborah A Tweddle, Helen E Bryant

Affiliations

  1. Academic Unit of Molecular Oncology, Department of Oncology and Metabolism, Sheffield Institute for Nucleic Acids (SInFoNiA), University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK.
  2. Wolfson Childhood Cancer Research Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
  3. Newcastle Centre for Cancer, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.
  4. Sheffield Children's Hospital, Western Bank, Sheffield S10 2TH, UK.

PMID: 34944835 PMCID: PMC8699051 DOI: 10.3390/cancers13246215

Abstract

Despite intensive high-dose multimodal therapy, high-risk neuroblastoma (NB) confers a less than 50% survival rate. This study investigates the role of replication stress in sensitivity to inhibition of Ataxia telangiectasia and Rad3-related (ATR) in pre-clinical models of high-risk NB. Amplification of the oncogene

Keywords: ATR; MYCN; PARP; neuroblastoma; replication stress

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