FoxO3 and oxidative stress: a multifaceted role in cellular adaptation.
Victoria Simões BernardoFlaviene Felix TorresDanilo Grünig Humberto da SilvaPublished in: Journal of molecular medicine (Berlin, Germany) (2023)
Oxidative stress is a major cause of morbidity and mortality in human health and disease. In this review, we focus on the Forkhead Box (Fox) subclass O3 (FoxO3), an extensively studied transcription factor that plays a pleiotropic role in a wide range of physiological and pathological processes by regulating multiple gene regulatory networks involved in the modulation of numerous aspects of cellular metabolism, including fuel metabolism, cell death, and stress resistance. This review will also focus on regulatory mechanisms of FoxO3 expression and activity, such as crucial post-translational modifications and non-coding RNAs. Moreover, this work discusses and evidences some pathways to how this transcription factor and reactive oxygen species regulate each other, which may lead to the pathogenesis of various types of diseases. Therefore, in addition to being a promising therapeutic target, the FoxO3-regulated signaling pathways can also be used as reliable diagnostic and prognostic biomarkers and indicators for drug responsiveness.
Keyphrases
- transcription factor
- oxidative stress
- human health
- cell death
- dna binding
- reactive oxygen species
- risk assessment
- signaling pathway
- dna damage
- induced apoptosis
- poor prognosis
- genome wide identification
- ischemia reperfusion injury
- climate change
- pi k akt
- multidrug resistant
- diabetic rats
- binding protein
- cell cycle arrest
- stress induced
- long non coding rna