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Expression of angiogenic factors in chronic myeloid leukaemia:: role of the bcr/abl oncogene, biochemical mechanisms, and potential clinical implications

Journal

EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
Volume 34, Issue -, Pages 2-11

Publisher

WILEY
DOI: 10.1111/j.0960-135X.2004.01365.x

Keywords

CML; BCR/ABL; VEGF; rapamycin

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Chronic myeloid leukaemia (CMC) is a stem cell disease characterized by an increased production and accumulation of clonal BCR/ABL-positive cells in haematopoietic tissues. The chronic phase of CML is inevitably followed by an accelerated phase of the disease, with consecutive blast crisis. However, depending on genetic stability, epigenetic events, and several other factors, the clinical course and survival appear to vary among patients. Recent data suggest that angiogenic cytokines such as vascular endothelial growth factor (VEGF), are up-regulated in CML, and play a role in the pathogenesis of the disease. These factors appear to be produced and released in leukaemic cells in patients with CML. In line with this notion, increased serum-levels of angiogenic growth factors are measurable in CAAL patients. In this study we provide an overview of angiogenic growth factors expressed in CML cells, discuss the possible pathogenetic role of these cytokines, the biochemical basis of their production in leukaemic cells, and their potential clinical implications.

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