4.5 Article

DNA-damaging autoantibodies and cancer: the lupus butterfly theory

Journal

NATURE REVIEWS RHEUMATOLOGY
Volume 12, Issue 7, Pages 429-434

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrrheum.2016.23

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Funding

  1. Biomedical Centre
  2. National Institutes of Health (NIH) [R03CA173822, P60 AR066464]
  3. Department of Therapeutic Radiology at Yale School of Medicine
  4. Yale Center for Clinical Investigation CTSA Scholar Award
  5. CTSA Grant from the National Center for Advancing Translational Science (NCATS), NIH [UL1 TR000142]
  6. University College London

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Autoantibodies reactive against host DNA are detectable in the circulation of most people with systemic lupus erythematosus (SLE). The long-held view that antibodies cannot penetrate live cells has been disproved. A subset of lupus autoantibodies penetrate cells, translocate to nuclei, and inhibit DNA repair or directly damages DNA. The result of these effects depends on the microenvironment and genetic traits of the cell. Some DNA-damaging antibodies alone have little impact on normal cells, but in the presence of other conditions, such as pre-existing DNA-repair defects, can become highly toxic. These findings raise new questions about autoimmunity and DNA damage, and reveal opportunities for new targeted therapies against malignancies particularly vulnerable to DNA damage. In this Perspectives article, we review the known associ-ations between SLE, DNA damage and cancer, and propose a theory for the effects of DNA-damaging autoantibodies on SLE pathophysiology and cancer risk.

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