Best Practice & Research Clinical Haematology
Volume 22, Issue 2 , Pages 181-190, June 2009

The impact of gene profiling in chronic myeloid leukaemia

  • Agnes S.M. Yong, MBBCh, MRCP (UK), FRCPath, PhD (Senior Research Fellow)

      Affiliations

    • Haematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda MD 20892, USA
  • ,
  • Junia V. Melo, MD, PhD, FRCPath (Professor)

      Affiliations

    • Division of Haematology, Institute of Medical & Veterinary Science, Frome Road, Adelaide, South Australia 5000, Australia
    • Corresponding Author InformationCorresponding author. Tel.: +61 8 8222 3441; Fax: +61 8 8222 3139.

The use of microarray technology in chronic myeloid leukaemia (CML) has increased our understanding of the biology of this disease. From early studies of gene expression profiling in BCR-ABL-positive cell lines to samples from patients in different disease phases of CML, using resting cells or cells treated with a variety of therapeutic agents, the field has now moved on to profiling microRNA and single nucleotide polymorphisms of CML cells. With the advent of tyrosine kinase inhibitors, several groups have also attempted to use microarray profiling to ascertain if particular gene expression profiles pre-existing in patients' CML cells, which could reflect intrinsic disease biology, would predict for response to treatment. This could streamline patients for alternative treatments upfront should a poor risk profile be found. In this article, we provide an overview of the progress made so far in this field, and outline the more substantial results of available microarray studies to date.

Keywords: chronic myeloid leukaemia, gene expression, microarray, molecular biology, BCR-ABL, tyrosine kinase

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PII: S1521-6926(09)00023-1

doi:10.1016/j.beha.2009.04.002

Best Practice & Research Clinical Haematology
Volume 22, Issue 2 , Pages 181-190, June 2009