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    Expression of pro-apoptotic Bfk isoforms reduces during malignant transformation in the human gastrointestinal tract.

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    Authors
    Dempsey, Clare E
    Dive, Caroline
    Fletcher, Daniel J
    Barnes, Frances A
    Lobo, Alan
    Bingle, Colin D
    Whyte, Moira K B
    Renshaw, Stephen A
    Affiliation
    Academic Unit of Respiratory Medicine, Division of Genomic Medicine, University of Sheffield, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, United Kingdom.
    Issue Date
    2005-07-04
    
    Metadata
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    Abstract
    Reduced expression of pro-apoptotic Bcl-2 family proteins has been described in many gastrointestinal cancers, and may play a role in tumourigenesis. The human homologue of the pro-apoptotic Bcl-2 protein, Bfk, is predominantly expressed in tissues of the gastrointestinal tract. In colon, four alternatively spliced isoforms were identified; of which two are pro-apoptotic when overexpressed. In the transition from normal tissue to tumour, pro-apoptotic Bfk isoform expression is substantially reduced in up to 80% of tumours isolated from the human gastrointestinal tract (8/10 colonic tumours and 26/37 of all gastrointestinal tumours) compared to 3/117 tumours from outside the gastrointestinal tract. These data suggest that pro-apoptotic isoforms of Bfk may help to protect against the development of human gastrointestinal malignancy.
    Citation
    Expression of pro-apoptotic Bfk isoforms reduces during malignant transformation in the human gastrointestinal tract. 2005, 579 (17):3646-50 FEBS Lett.
    Journal
    FEBS Letters
    URI
    http://hdl.handle.net/10541/75634
    DOI
    10.1016/j.febslet.2005.05.050
    PubMed ID
    15961081
    Type
    Article
    Language
    en
    ISSN
    0014-5793
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.febslet.2005.05.050
    Scopus Count
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    All Paterson Institute for Cancer Research

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