A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups

Sarina Sulong, Anthony V. Moorman, Julie A.E. Irving, Jonathan C. Strefford, Zoe J. Konn, Marian C. Case, Lynne Minto, Kerry E. Barber, Helen Parker, Sarah L. Wright, Adam R.M. Stewart, Simon Bailey, Nick P. Bown, Andrew G. Hall, Christine J. Harrison

Research output: Contribution to journalArticle

Abstract

Inactivation of the tumor suppressor gene, CDKN2A, can occur by deletion, methylation, or mutation. We assessed the principal mode of inactivation in childhood acute lymphoblastic leukemia (ALL) and frequency in biologically relevant subgroups. Mutation or methylation was rare, whereas genomic deletion occurred in 21% of B-cell precursor ALL and 50% of T-ALL patients. Single nucleotide polymorphism arrays revealed copy number neutral (CNN) loss of heterozygosity (LOH) in 8% of patients. Array-based comparative genomic hybridization demonstrated that the mean size of deletions was 14.8 Mb and biallelic deletions composed a large and small deletion (mean sizes, 23.3 Mb and 1.4 Mb). Among 86 patients, only 2 small deletions were below the resolution of detection by fluorescence in situ hybridization. Patients with high hyperdiploidy, ETV6-RUNX1, or 11q23/MLL rearrangements had low rates of deletion (11%, 15%, 13%), whereas patients with t(9;22), t(1;19), TLX3, or TLX1 rearrangements had higher frequencies (61%, 42%, 78%, and 89%). In conclusion, CDKN2A deletion is a significant secondary abnormality in childhoodALL strongly correlated with phenotype and genotype. The variation in the incidence of CDKN2A deletions by cytogenetic subgroup may explain its inconsistent association with outcome. CNN LOH without apparent CDKN2A inactivation suggests the presence of other relevant genes in this region.

Original languageEnglish (US)
Pages (from-to)100-107
Number of pages8
JournalBlood
Volume113
Issue number1
DOIs
StatePublished - Jan 1 2009

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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    Sulong, S., Moorman, A. V., Irving, J. A. E., Strefford, J. C., Konn, Z. J., Case, M. C., Minto, L., Barber, K. E., Parker, H., Wright, S. L., Stewart, A. R. M., Bailey, S., Bown, N. P., Hall, A. G., & Harrison, C. J. (2009). A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups. Blood, 113(1), 100-107. https://doi.org/10.1182/blood-2008-07-166801