4.8 Article

The Genetic Landscape of the Childhood Cancer Medulloblastoma

Journal

SCIENCE
Volume 331, Issue 6016, Pages 435-439

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1198056

Keywords

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Funding

  1. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  2. Virginia and D. K. Ludwig Fund for Cancer Research
  3. Alex's Lemonade Stand Foundation
  4. American Brain Tumor Association
  5. Brain Tumor Research Fund at Johns Hopkins
  6. Hoglund Foundation
  7. Ready or Not Foundation
  8. Children's Brain Tumor Foundation
  9. Pediatric Brain Tumor Foundation Institute
  10. David and Barbara B. Hirschhorn Foundation
  11. American Association for Cancer Research
  12. Johns Hopkins Sommer Scholar Program
  13. NIH [CA121113, CA096832, CA057345, CA118822, CA135877, GM074906-01A1/B7BSCW]
  14. NSF [DBI 0845275]
  15. DOD NDSEG [32 CFR 168a]
  16. Direct For Biological Sciences
  17. Div Of Biological Infrastructure [0845275] Funding Source: National Science Foundation

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Medulloblastoma (MB) is the most common malignant brain tumor of children. To identify the genetic alterations in this tumor type, we searched for copy number alterations using high-density microarrays and sequenced all known protein-coding genes and microRNA genes using Sanger sequencing in a set of 22 MBs. We found that, on average, each tumor had 11 gene alterations, fewer by a factor of 5 to 10 than in the adult solid tumors that have been sequenced to date. In addition to alterations in the Hedgehog and Wnt pathways, our analysis led to the discovery of genes not previously known to be altered in MBs. Most notably, inactivating mutations of the histone-lysine N-methyltransferase genes MLL2 or MLL3 were identified in 16% of MB patients. These results demonstrate key differences between the genetic landscapes of adult and childhood cancers, highlight dysregulation of developmental pathways as an important mechanism underlying MBs, and identify a role for a specific type of histone methylation in human tumorigenesis.

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