Significance of chromosomal alterations and mutations of the N-RAS and TP53 genes in relation to leukemogenesis of acute myeloid leukemia

Leuk Res. 1998 Jul;22(7):631-7. doi: 10.1016/s0145-2126(98)00056-3.

Abstract

We examined chromosomes and mutations of the N-RAS and TP53 genes in 73 patients with acute myeloid leukemia (AML). Twenty-six patients showed a reciprocal chromosomal translocation or an inversion, and 34 patients showed only unbalanced aberrations. Balanced aberrations were predominantly detected in the AML patients who did not have myelodysplasia, preceding myelodysplastic syndrome, and a history of chemotherapy or radiation therapy. In contrast, unbalanced aberrations were more frequently seen in the patients with AML with trilineage myelodysplasia, AML transformed from MDS, and therapy-related AML. Twenty-two mutations of the N-RAS and TP53 genes were detected, and these mutations were frequently associated with unbalanced chromosomal aberrations. Furthermore, the spectrum of mutations was suggestive of an exposure to alkylating chemicals.

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Aged, 80 and over
  • Chromosome Aberrations / genetics
  • Chromosomes / genetics*
  • Chromosomes, Human, Pair 17 / genetics
  • Chromosomes, Human, Pair 5 / genetics
  • Chromosomes, Human, Pair 7 / genetics
  • Female
  • Genes, p53 / genetics*
  • Genes, ras / genetics*
  • Humans
  • Karyotyping
  • Leukemia, Myeloid / classification
  • Leukemia, Myeloid / etiology*
  • Leukemia, Myeloid / genetics*
  • Male
  • Middle Aged
  • Mutation / genetics*