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    Autoantibodies and cancer among asbestos-exposed cohorts in Western Australia

    92827.pdf (284.0Kb)
    Access Status
    Open access
    Authors
    Carey, Renee
    Pfau, J.C.
    Fritzler, M.J.
    Creaney, J.
    de Klerk, N.
    Musk, A. W. (Bill)
    Franklin, P.
    Sodhi-Berry, N.
    Brims, Fraser
    Reid, Alison
    Date
    2021
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Carey, R.N. and Pfau, J.C. and Fritzler, M.J. and Creaney, J. and de Klerk, N. and W (Bill) Musk, A. and Franklin, P. et al. 2021. Autoantibodies and cancer among asbestos-exposed cohorts in Western Australia. Journal of Toxicology and Environmental Health - Part A: Current Issues. 84 (11): pp. 475-483.
    Source Title
    Journal of Toxicology and Environmental Health - Part A: Current Issues
    DOI
    10.1080/15287394.2021.1889424
    ISSN
    1528-7394
    Faculty
    Faculty of Health Sciences
    School
    Curtin School of Population Health
    Curtin Medical School
    Remarks

    This is an Accepted Manuscript of an article published by Taylor & Francis in Journal of Toxicology and Environmental Health, Part A: Current Issues on 07 Mar 2021, available at: https://doi.org/10.1080/15287394.2021.1889424.

    URI
    http://hdl.handle.net/20.500.11937/93003
    Collection
    • Curtin Research Publications
    Abstract

    Asbestos exposure is associated with many adverse health conditions including malignant mesothelioma and lung cancer as well as production of autoantibodies. Autoantibodies may serve as biomarkers for asbestos exposure in patients with cancer, and autoimmune dysfunction has been linked to increased rates of various cancers. The aim of this study was to examine the hypothesis that autoantibodies are more frequent in asbestos-exposed individuals with either lung cancer or mesothelioma than those without these conditions. Asbestos-exposed individuals from Western Australia who had lung cancer (n = 24), malignant mesothelioma (n = 24), or no malignancy (n = 51) were tested for antinuclear autoantibodies (ANA) using indirect immunofluorescence and specific extractable nuclear autoantibodies (ENA) employing a multiplexed addressable laser bead immunoassay. Contrary to the hypothesis, data demonstrated that individuals without malignancy were more likely to be positive for ANA compared to those with cancer. However, autoantibodies to histone and Ro-60 were found to be associated with lung cancer. These results support a possible predictive value for specific autoantibodies in the early detection of lung cancer and/or in our understanding of the role of autoimmune processes in cancer. However, further studies are needed to identify specific target antigens for the antibodies.

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