A “FOXO” in sight: Targeting Foxo proteins from conception to cancer
- 4 November 2008
- journal article
- review article
- Published by Wiley in Medicinal Research Reviews
- Vol. 29 (3) , 395-418
- https://doi.org/10.1002/med.20139
Abstract
The successful treatment for multiple disease entities can rest heavily upon the ability to elucidate the intricate relationships that govern cellular proliferation, metabolism, survival, and inflammation. Here we discuss the therapeutic potential of the mammalian forkhead transcription factors predominantly in the O class, FoxO1, FoxO3, FoxO4, and FoxO6, which play a significant role during normal cellular function as well as during progressive disease. These transcription factors are integrated with several signal transduction pathways, such as Wnt proteins, that can regulate a broad array of cellular process that include stem cell proliferation, aging, and malignancy. FoxO transcription factors are attractive considerations for strategies directed against human cancer in light of their pro‐apoptotic effects and ability to lead to cell cycle arrest. Yet, FoxO proteins can be associated with infertility, cellular degeneration, and unchecked cellular proliferation. As our knowledge continues to develop for this novel family of proteins, potential clinical applications for the FoxO family should heighten our ability to limit disease progression without clinical compromise. © 2008 Wiley periodicals, Inc. Med Res Rev, 29, No. 3, 395‐418, 2009Keywords
This publication has 182 references indexed in Scilit:
- OutFOXOing disease and disability: the therapeutic potential of targeting FoxO proteinsTrends in Molecular Medicine, 2008
- Triple play: Promoting neurovascular longevity with nicotinamide, WNT, and erythropoietin in diabetes mellitusBiomedicine & Pharmacotherapy, 2008
- Erythropoietin: Elucidating new cellular targets that broaden therapeutic strategiesProgress in Neurobiology, 2008
- Raves and risks for erythropoietinCytokine & Growth Factor Reviews, 2008
- Differential cleavage of Mst1 by caspase-7/-3 is responsible for TRAIL-induced activation of the MAPK superfamilyCellular Signalling, 2008
- FoxO tumor suppressors and BCR–ABL-induced leukemia: A matter of evasion of apoptosisBiochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2008
- Cellular demise and inflammatory microglial activation during β-amyloid toxicity are governed by Wnt1 and canonical signaling pathwaysCellular Signalling, 2007
- FoxOs Are Lineage-Restricted Redundant Tumor Suppressors and Regulate Endothelial Cell HomeostasisCell, 2007
- A Conserved MST-FOXO Signaling Pathway Mediates Oxidative-Stress Responses and Extends Life SpanCell, 2006
- New Avenues of Exploration for ErythropoietinJAMA, 2005