Novel therapies for chronic myelogenous leukemia

Exp Hematol. 2001 May;29(5):543-56. doi: 10.1016/s0301-472x(01)00633-6.

Abstract

The BCR-ABL oncogene is essential to the pathogenesis of chronic myelogenous leukemia, and immune mechanisms play an important role in control of this disease. Understanding of the molecular pathogenesis of chronic myelogenous leukemia has led to the development of several novel therapies, which can be broadly divided into therapies based on 1) inhibition of the BCR-ABL oncogene expression, 2) inhibition of other genes important to the pathogenesis of chronic myelogenous leukemia, 3) inhibition of BCR-ABL protein function, and 4) immunomodulation. We have systematically reviewed each of these novel therapeutic approaches in this article.

Publication types

  • Review

MeSH terms

  • Alkyl and Aryl Transferases / antagonists & inhibitors
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Benzamides
  • Cancer Vaccines / therapeutic use
  • Cell Transformation, Neoplastic / genetics
  • Clinical Trials, Phase II as Topic
  • Clinical Trials, Phase III as Topic
  • Drug Resistance, Neoplasm / genetics
  • Enzyme Inhibitors / therapeutic use
  • Farnesyltranstransferase
  • Fusion Proteins, bcr-abl / antagonists & inhibitors
  • Fusion Proteins, bcr-abl / genetics
  • Fusion Proteins, bcr-abl / physiology
  • Genes, myb
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Imatinib Mesylate
  • Immunotherapy, Adoptive
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / therapy
  • Methotrexate / pharmacology
  • Models, Biological
  • Multicenter Studies as Topic
  • Neoplasm Proteins / metabolism
  • Oligonucleotides, Antisense / pharmacology
  • Oligonucleotides, Antisense / therapeutic use
  • Phosphorylation
  • Piperazines / pharmacology
  • Piperazines / therapeutic use
  • Protein Processing, Post-Translational
  • Pyrimidines / pharmacology
  • Pyrimidines / therapeutic use
  • RNA, Messenger / antagonists & inhibitors
  • RNA, Neoplasm / antagonists & inhibitors
  • Signal Transduction / drug effects
  • Tetrahydrofolate Dehydrogenase / genetics

Substances

  • Antineoplastic Agents
  • Benzamides
  • Cancer Vaccines
  • Enzyme Inhibitors
  • Neoplasm Proteins
  • Oligonucleotides, Antisense
  • Piperazines
  • Pyrimidines
  • RNA, Messenger
  • RNA, Neoplasm
  • Imatinib Mesylate
  • Tetrahydrofolate Dehydrogenase
  • Alkyl and Aryl Transferases
  • Farnesyltranstransferase
  • Fusion Proteins, bcr-abl
  • Methotrexate