Clonal evolution to acute myeloblastic leukemia with MLL gene rearrangement from trisomy 8 clone

Leukemia. 1997 Aug;11(8):1380-2. doi: 10.1038/sj.leu.2400708.

Abstract

A 20-year-old Japanese man was referred because of severe pancytopenia with 14% of abnormal blasts in hypocellular bone marrow. After treatment by granulocyte colony-stimulating factor (G-CSF) and transfusions of red blood cells, spontaneous remission was subsequently achieved. After 3 months' remission, however, the patient developed AML characterized by the abnormal karyotype: 46XY,+8,t(9;11)(p22;q23). FISH study revealed the presence of trisomy 8 clone also in the hypoplastic state. While MLL-AF9 chimeric mRNA was observed in leukemic cells, it was not detectable in bone marrow cells from the hypoplastic state by RT-PCR. This is the first report of a trisomy 8 clone which evolved into one with a MLL gene rearrangement.

Publication types

  • Letter

MeSH terms

  • Chromosomes, Human, Pair 21*
  • DNA-Binding Proteins / genetics*
  • Histone-Lysine N-Methyltransferase
  • Humans
  • In Situ Hybridization, Fluorescence
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / pathology*
  • Male
  • Myelodysplastic Syndromes / genetics*
  • Myeloid-Lymphoid Leukemia Protein
  • Nuclear Proteins / genetics
  • Proto-Oncogenes*
  • Transcription Factors*
  • Translocation, Genetic
  • Trisomy*

Substances

  • DNA-Binding Proteins
  • KMT2A protein, human
  • MLLT3 protein, human
  • Nuclear Proteins
  • Transcription Factors
  • Myeloid-Lymphoid Leukemia Protein
  • Histone-Lysine N-Methyltransferase