NOTCH1 mutation in a female with myeloid/NK cell precursor acute leukemia

Pediatr Blood Cancer. 2010 Dec 15;55(7):1406-9. doi: 10.1002/pbc.22758.

Abstract

A 6-year-old Japanese female was diagnosed as having myeloid/NK cell precursor acute leukemia (MNKL) using immunocytochemical analysis. The patient was treated by cord blood transplantation from an HLA 1-locus mismatched unrelated donor after chemotherapy comprising cytosine arabinoside, idarubicin, etoposide, and L-asparaginase. We detected a nonsense mutation, C7412A, resulting in S2471X, where X is a terminal codon, in the PEST domain of NOTCH1 in this patient. The presence of the NOTCH1 activating mutation in MNKL might suggest a possible role in the leukemogenesis of MNKL.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Agents
  • Asparaginase / therapeutic use
  • Child
  • Codon, Nonsense*
  • Cord Blood Stem Cell Transplantation
  • Female
  • Humans
  • Killer Cells, Natural*
  • Leukemia, Myeloid, Acute / genetics*
  • Leukemia, Myeloid, Acute / therapy
  • Receptor, Notch1 / genetics*

Substances

  • Antineoplastic Agents
  • Codon, Nonsense
  • Receptor, Notch1
  • Asparaginase