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    bcl-2 delay of alkylating agent-induced apoptotic death in a murine hemopoietic stem cell line.

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    Authors
    Fairbairn, Leslie J
    Cowling, Graham J
    Dexter, T Michael
    Rafferty, Joseph A
    Margison, Geoffrey P
    Reipert, Brigit M
    Affiliation
    CRC Department of Experimental Haematology, Paterson Institute for Cancer Research, Christie Hospital National Health Service Trust, Manchester, United Kingdom.
    Issue Date
    1994-09
    
    Metadata
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    Abstract
    Many cytotoxic agents kill cells by invoking a specific death pathway termed physiological cell death, or apoptosis. Treatment of a murine hemopoietic stem cell line, FDCP-mix, with methylmethanesulfonate (MMS) or N'-methyl-N'-nitrosourea (MNU) leads to death by apoptosis. Retroviral gene transfer was used to overexpress the bcl-2 oncogene in FDCP-mix cells, and this was associated with a delay in apoptosis in these cells after treatment with MNU and MMS and decreased sensitivity of colony formation to the cytotoxic effects of MMS. These data suggest an explanation for the refractory nature of bcl-2-expressing follicular lymphoma to cytotoxic chemotherapy and furthermore suggest that DNA-damaging antitumor therapy may contribute to the progression of disease.
    Citation
    bcl-2 delay of alkylating agent-induced apoptotic death in a murine hemopoietic stem cell line. 1994, 11 (1):49-55 Mol. Carcinog.
    Journal
    Molecular Carcinogenesis
    URI
    http://hdl.handle.net/10541/96943
    DOI
    10.1002/mc.2940110109
    PubMed ID
    7916990
    Type
    Article
    Language
    en
    ISSN
    0899-1987
    ae974a485f413a2113503eed53cd6c53
    10.1002/mc.2940110109
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research

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