Monitoring AML1-ETO and CBFbeta-MYH11 transcripts in acute myeloid leukemia

Curr Oncol Rep. 2003 Sep;5(5):399-404. doi: 10.1007/s11912-003-0026-6.

Abstract

The core-binding factor (CBF) leukemias comprise acute myeloid leukemia (AML) with t(8;21) and inv(16)/t(16;16), characterized by the presence of the AML1-ETO and CBFbeta-MYH11 fusion genes, respectively. These leukemia-associated genes can now be sensitively and reliably quantified by real-time reverse transcription polymerase chain reaction (RT-PCR) techniques and thus can serve as molecular targets for monitoring residual leukemia. Studies to date suggest that quantitative monitoring of minimal residual disease (MRD) in CBF-positive AML is useful in distinguishing patients at high risk of relapse from those in durable remission. Preliminary results of MRD monitoring by real-time RT-PCR in this subset of AML patients are promising and provide the basis for further evaluation by quantitative analysis in large prospective clinical trials.

MeSH terms

  • Acute Disease
  • Core Binding Factor Alpha 2 Subunit
  • Humans
  • Leukemia, Myeloid / metabolism*
  • Leukemia, Myeloid / therapy
  • Monitoring, Physiologic
  • Neoplasm, Residual
  • Oncogene Proteins, Fusion / genetics
  • Oncogene Proteins, Fusion / metabolism*
  • Polymerase Chain Reaction
  • Prognosis
  • RNA, Neoplasm / metabolism
  • RUNX1 Translocation Partner 1 Protein
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • AML1-ETO fusion protein, human
  • CBFbeta-MYH11 fusion protein
  • Core Binding Factor Alpha 2 Subunit
  • Oncogene Proteins, Fusion
  • RNA, Neoplasm
  • RUNX1 Translocation Partner 1 Protein
  • Transcription Factors