articleBloodMay 12, 2007BRONZE OA

Bcr-Abl kinase domain mutations, drug resistance, and the road to a cure for chronic myeloid leukemia

Howard Hughes Medical Institute · Oregon Health & Science University

PubMed
Indexed incrossrefpubmed

Abstract

Mutations in the kinase domain (KD) of BCR-ABL are the most prevalent mechanism of acquired imatinib resistance in patients with chronic myeloid leukemia (CML). Here we examine predisposing factors underlying acquisition of KD mutations, evidence for acquisition of mutations before and during therapy, and whether the detection of a KD mutation universally implies resistance. We also provide a perspective on how the second-line Abl inhibitors dasatinib and nilotinib are faring in the treatment of imatinib-resistant CML, especially in relation to specific KD mutations. We discuss the growing importance of the multi-inhibitor-resistant 315T>I mutant and the therapeutic potential that a 315T>I inhibitor would…

Citation impact

640
total citations
FWCI
26.48
Percentile
100%
References
59
Citations per year

Authors

3

Topics & keywords

Keywords
  • Nilotinib
  • Dasatinib
  • Imatinib
  • Myeloid leukemia
  • Cancer research
  • Context (archaeology)
  • Protein kinase domain
  • Mutation
UN Sustainable Development Goals
  • Good health and well-being
No related works found for this paper.