Both NUP98/TOP1 and TOP1/NUP98 transcripts are detected in a de novo AML with t(11;20)(p15;q11)

Genes Chromosomes Cancer. 2003 Sep;38(1):102-5. doi: 10.1002/gcc.10239.

Abstract

The NUP98 gene is involved in several chromosomal abnormalities associated with acute leukemia. The recurrent t(11;20)(p15;q11) chromosomal translocation results in generation of the NUP98/TOP1 chimeric gene. This abnormality has been observed primarily in therapy-related leukemias, and TOP1/NUP98 transcripts have not been demonstrated. We describe a case of de novo acute myeloid leukemia with t(11;20)(p15;q11), with no known history of exposure to chemicals. The translocation occurred in intron 13 of NUP98 and intron 7 of TOP1, as in the three previously reported cases. The breakpoint in NUP98 was exactly the same as that found in a previously reported case. In addition, a reciprocal TOP1/NUP98 transcript was detected for the first time in our patient.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Base Sequence / genetics
  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 20 / genetics*
  • DNA Topoisomerases, Type I / genetics*
  • DNA, Neoplasm / genetics
  • Female
  • Humans
  • Leukemia, Myeloid / genetics*
  • Middle Aged
  • Molecular Sequence Data
  • Nuclear Pore Complex Proteins / genetics*
  • Oncogene Proteins, Fusion / genetics*
  • Translocation, Genetic / genetics*

Substances

  • DNA, Neoplasm
  • NUP98-TOP1 fusion protein, human
  • Nuclear Pore Complex Proteins
  • Oncogene Proteins, Fusion
  • nuclear pore complex protein 98
  • DNA Topoisomerases, Type I