Alterations of the AML1 transcription factor in human leukemia

Semin Cell Dev Biol. 2000 Oct;11(5):347-60. doi: 10.1006/scdb.2000.0183.

Abstract

The identification of clonal chromosomal translocations in human leukemias provided one of the first insights into the underlying pathogenesis of this clinically heterogeneous disease. Over the last decade a large number of these chromosomal rearrangements have been molecularly cloned and the involved genes identified. A surprising finding that has emerged from this work is that many of these chromosomal alterations target the genes encoding the AML1/CBFbeta transcription factor complex, a critical regulator of normal hematopoiesis. In this review, we summarize our present understanding of the mechanisms through which alterations of AML1/CBFbeta contribute to leukemogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Acute Disease
  • Animals
  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Leukemic
  • Hematopoiesis
  • Hematopoietic Stem Cells / physiology*
  • Humans
  • Leukemia / etiology*
  • Leukemia / genetics
  • Leukemia, Myeloid / genetics
  • Oncogene Proteins, Fusion / genetics*
  • Oncogene Proteins, Fusion / metabolism
  • Point Mutation
  • Proto-Oncogene Proteins*
  • RUNX1 Translocation Partner 1 Protein
  • Transcription Factor AP-2
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Translocation, Genetic*

Substances

  • Core Binding Factor Alpha 2 Subunit
  • DNA-Binding Proteins
  • Oncogene Proteins, Fusion
  • Proto-Oncogene Proteins
  • RUNX1 Translocation Partner 1 Protein
  • RUNX1 protein, human
  • RUNX1T1 protein, human
  • Transcription Factor AP-2
  • Transcription Factors