Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis

Cancer Genet Cytogenet. 2001 Jul 15;128(2):114-9. doi: 10.1016/s0165-4608(01)00412-5.

Abstract

A major deletion of the region proximal to the rearranged ABL gene on 9q was found in 14/94 (15%) of chronic myelogenous leukemia Philadelphia-positive patients by interphase fluorescent in situ hybridization with the BCR/ABL extra signal dual-color probe. Preliminary results indicated that the prognosis of the deletion 9q patients is probably worse than that of the non-deletion 9q patients. Twelve of the 14 deletion 9q patients were treated with alpha-interferon and none had a major cytogenetic response. The median duration of the chronic phase in patients not undergoing BMT was significantly shorter for the deletion 9q patients as compared to the non-deletion 9q patients (p =.0144). DNA microarray technology was performed in order to compare the gene expression patterns between the two groups of patients. A number of genes exhibiting differential expression, especially involving cell adhesion and migration, were identified. This finding may identify a sub-group of CML patients with different cell properties and a relatively poor prognosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Chromosomes, Human, Pair 9 / genetics*
  • Drug Resistance, Neoplasm / genetics
  • Gene Deletion*
  • Gene Expression Profiling
  • Gene Expression Regulation, Leukemic / genetics
  • Genes, abl*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Interferon-alpha / therapeutic use*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
  • Oligonucleotide Array Sequence Analysis
  • Prognosis
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics

Substances

  • Antineoplastic Agents
  • Interferon-alpha
  • RNA, Messenger