Mechanisms of Disease Persistence in Chronic Myelogenous Leukemia

Abstract

Disease persistence is the main issue faced by CML patients on therapy with imatinib and eradication of persistent malignant cells will be critical for the long-term success of kinase inhibitor therapy. Mechanisms underlying acquired resistance to imatinib have been extensively studied and the manner by which mutations of the Bcr-Abl kinase domain can reduce or eliminate sensitivity of CML cells to imatinib has been well characterized. Disease persistence in responding patients, in contrast,is still poorly understood. We sought to identify and extensively characterize hematopoietic stem cells responsible for disease persistence and explore their mechanisms of imatinib resistance. Using in vitro culture of primary CML progenitor cells, we identified both quiescent and cycling cells capable of surviving in the presence of imatinib. We observed inhibition of tyrosine phosphorylation by imatinib in phenotypically-defined CML stem cells and quiescent stem cells, and cells surviving in vitro culture, suggesting a Bcr-Abl independent mechanism of survival. To apply information gained from in vitro culture to persistent cell populations in treated CML patients, we attempted to isolate Bcr-Abl positive cells from patients in cytogenetic remission. Although persistent CML cells may reside within the stem cell compartment, techniques of stem cell enrichment did not lead to enrichment of CML cells. We therefore explored techniques for Bcr-Abl-specific detection to facilitate these studies, including creation of a Bcr-Abl junction-specific antibody, development of a Bcr-Abl mRNA junction-specific molecular beacon and analysis of potential markers of CML cells. The detailed analysis of primary samples is technically challenging, but is essential for an understanding of disease persistence and may allow identification of novel drug targets or methods to sensitize resistant cells to imatinib or alternative Bcr-Abl kinase inhibitors.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2007
Accession Number
ADA482232

Entities

People

  • Brian J. Druker
  • Richard L. Defoe

Organizations

  • University of Oregon

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Bone Marrow
  • Bone Marrow Cells
  • Cell Physiological Processes
  • Cells
  • Detection
  • Diseases And Disorders
  • Inhibition
  • Inhibitors
  • Kinases
  • Proteins
  • Resistance
  • Sensitivity
  • Stem Cells
  • Survival
  • Target Recognition
  • Tyrosine

Fields of Study

  • Biology
  • Medicine

Readers

  • Breast cancer cell signaling and growth regulation.
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology