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Diagnostic classification of childhood cancer using multiscale transcriptomics.
Comitani, Federico; Nash, Joshua O; Cohen-Gogo, Sarah; Chang, Astra I; Wen, Timmy T; Maheshwari, Anant; Goyal, Bipasha; Tio, Earvin S; Tabatabaei, Kevin; Mayoh, Chelsea; Zhao, Regis; Ho, Ben; Brunga, Ledia; Lawrence, John E G; Balogh, Petra; Flanagan, Adrienne M; Teichmann, Sarah; Huang, Annie; Ramaswamy, Vijay; Hitzler, Johann; Wasserman, Jonathan D; Gladdy, Rebecca A; Dickson, Brendan C; Tabori, Uri; Cowley, Mark J; Behjati, Sam; Malkin, David; Villani, Anita; Irwin, Meredith S; Shlien, Adam.
Affiliation
  • Comitani F; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Nash JO; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Cohen-Gogo S; Laboratory of Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
  • Chang AI; Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
  • Wen TT; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Maheshwari A; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Goyal B; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Tio ES; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Tabatabaei K; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Mayoh C; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Zhao R; Children's Cancer Institute, Lowy Cancer Research Centre, UNSW Sydney, Sydney, NSW, Australia.
  • Ho B; School of Clinical Medicine, UNSW Sydney, Sydney, NSW, Australia.
  • Brunga L; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Lawrence JEG; Laboratory of Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
  • Balogh P; The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.
  • Flanagan AM; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Teichmann S; Wellcome Sanger Institute, Hinxton, UK.
  • Huang A; Department of Cellular and Molecular Pathology, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, UK.
  • Ramaswamy V; Department of Cellular and Molecular Pathology, Royal National Orthopaedic Hospital, Brockley Hill, Stanmore, UK.
  • Hitzler J; Research Department of Pathology, University College London Cancer Institute, London, UK.
  • Wasserman JD; Wellcome Sanger Institute, Hinxton, UK.
  • Gladdy RA; Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
  • Dickson BC; The Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children, Toronto, ON, Canada.
  • Tabori U; Medical Biophysics, University of Toronto, Toronto, ON, Canada.
  • Cowley MJ; Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
  • Behjati S; Medical Biophysics, University of Toronto, Toronto, ON, Canada.
  • Malkin D; Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
  • Villani A; Program in Developmental and Stem Cell Biology, The Hospital for Sick Children Research Institute, Toronto, ON, Canada.
  • Irwin MS; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
  • Shlien A; Department of Paediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
Nat Med ; 29(3): 656-666, 2023 03.
Article de En | MEDLINE | ID: mdl-36932241
ABSTRACT
The causes of pediatric cancers' distinctiveness compared to adult-onset tumors of the same type are not completely clear and not fully explained by their genomes. In this study, we used an optimized multilevel RNA clustering approach to derive molecular definitions for most childhood cancers. Applying this method to 13,313 transcriptomes, we constructed a pediatric cancer atlas to explore age-associated changes. Tumor entities were sometimes unexpectedly grouped due to common lineages, drivers or stemness profiles. Some established entities were divided into subgroups that predicted outcome better than current diagnostic approaches. These definitions account for inter-tumoral and intra-tumoral heterogeneity and have the potential of enabling reproducible, quantifiable diagnostics. As a whole, childhood tumors had more transcriptional diversity than adult tumors, maintaining greater expression flexibility. To apply these insights, we designed an ensemble convolutional neural network classifier. We show that this tool was able to match or clarify the diagnosis for 85% of childhood tumors in a prospective cohort. If further validated, this framework could be extended to derive molecular definitions for all cancer types.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Child / Humans Langue: En Journal: Nat Med Sujet du journal: BIOLOGIA MOLECULAR / MEDICINA Année: 2023 Type de document: Article Pays d'affiliation: Canada

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Child / Humans Langue: En Journal: Nat Med Sujet du journal: BIOLOGIA MOLECULAR / MEDICINA Année: 2023 Type de document: Article Pays d'affiliation: Canada