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    Loss of the Alox5 gene impairs leukemia stem cells and prevents chronic myeloid leukemia

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    Authors
    Chen, Yaoyu
    Hu, Yiguo
    Zhang, Haojian
    Peng, Cong
    Li, Shaoguang
    Student Authors
    Haojian Zhang
    UMass Chan Affiliations
    Department of Medicine, Division of Hematology/Oncology
    Document Type
    Journal Article
    Publication Date
    2009-07-01
    Keywords
    Carrier Proteins; Membrane Proteins; Neoplastic Stem Cells; Leukemia, Myelogenous, Chronic, BCR-ABL Positive
    Cancer Biology
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887745/pdf/nihms115650.pdf
    Abstract
    Targeting of cancer stem cells is believed to be essential for curative therapy of cancers, but supporting evidence is limited. Few selective target genes in cancer stem cells have been identified. Here we identify the arachidonate 5-lipoxygenase (5-LO) gene (Alox5) as a critical regulator for leukemia stem cells (LSCs) in BCR-ABL-induced chronic myeloid leukemia (CML). In the absence of Alox5, BCR-ABL failed to induce CML in mice. This Alox5 deficiency caused impairment of the function of LSCs but not normal hematopoietic stem cells (HSCs) through affecting differentiation, cell division and survival of long-term LSCs (LT-LSCs), consequently causing a depletion of LSCs and a failure of CML development. Treatment of CML mice with a 5-LO inhibitor also impaired the function of LSCs similarly by affecting LT-LSCs, and prolonged survival. These results demonstrate that a specific target gene can be found in cancer stem cells and its inhibition can completely inhibit the function of these stem cells.
    Source
    Nat Genet. 2009 Jul;41(7):783-92. Epub 2009 Jun 7. Link to article on publisher's website
    DOI
    10.1038/ng.389
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/33050
    PubMed ID
    19503090
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1038/ng.389
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