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OutFOXOing disease and disability: the therapeutic potential of targeting FoxO proteins

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 14, Issue 5, Pages 219-227

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2008.03.002

Keywords

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Funding

  1. NIEHS NIH HHS [P30 ES006639] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS053946-01A2, R01 NS053946, R01 NS053946-02] Funding Source: Medline

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Forkhead transcription factors have a 'winged helix' domain and regulate processes that range from cell longevity to cell death. Of the mammalian forkhead family members in the O class, FoxO1, FoxO3a and FoxO4 can fill a crucial void for the treatment of disorders that include aging, cancer, diabetes, infertility, neurodegeneration and immune system dysfunction. Yet, observations that forkhead family members also can compromise clinical utility have fueled controversy and highlight the necessity to further outline the integrated cellular pathways governed by these transcription factors. Here we discuss recent advances that have elucidated the unique cellular pathways and clinical potential of targeting FoxO proteins to develop novel therapeutic strategies and avert potential pitfalls that might be closely intertwined with its benefits for patient care.

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