Apurinic/apyrimidinic endonuclease 1 (APE1) is a multifunctional enzyme involved in the base excision repair (BER) pathway, which repairs oxidative base damage caused by endogenous and exogenous agents. APE1 acts as a reductive activator of many transcription factors (TFs) and has also been named redox effector factor 1, Ref-1. For example, APE1 activates activator protein-1, nuclear factor kappa B, hypoxia-inducible factor 1α, paired box gene 8, signal transducer activator of transcription 3 and p53, which are involved in apoptosis, inflammation, angiogenesis and survival pathways. APE1/Ref-1 maintains cellular homeostasis (redox) via the activation of TFs that regulate various physiological processes and that crosstalk with redox balancing agents (for example, thioredoxin, catalase and superoxide dismutase) by controlling levels of reactive oxygen and nitrogen species. The efficiency of APE1/Ref-1’s function(s) depends on pairwise interaction with participant protein(s), the functions regulated by APE1/Ref-1 include the BER pathway, TFs, energy metabolism, cytoskeletal elements and stress-dependent responses. Thus, APE1/Ref-1 acts as a ‘hub-protein’ that controls pathways that are important for cell survival. In this review, we will discuss APE1/Ref-1’s versatile nature in various human etiologies, including neurodegeneration, cancer, cardiovascular and other diseases that have been linked with alterations in the expression, subcellular localization and activities of APE/Ref-1. APE1/Ref-1 can be targeted for therapeutic intervention using natural plant products that modulate the expression and functions of APE1/Ref-1. In addition, studies focusing on translational applications based on APE1/Ref-1-mediated therapeutic interventions are discussed. Researchers in India review a multifunctional enzyme's role in various human diseases and some plant-derived compounds that may modify its behavior. Apurinic/apyrimidinic endonuclease (APE1) is best known for its role in repairing DNA that has suffered chemical damage. It is also involved in the regulation of gene expression. Anil Mantha and colleagues at the Central University of Punjab have described how these functions contribute to APE1 involvement in various pathologies. For example, while APE1 may help lessen damage to brain cells in neurodegenerative disorders like Alzheimer's disease, its DNA repair activity can protect deadly cancer cells from the lethal effects of chemotherapeutic drugs. Therapeutics that target APE1 are under development. The authors highlight a number of plant-derived compounds such as resveratrol and soy isoflavones that could prove helpful in manipulating APE1 activities.
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Thakur et al. (2014) studied this question.
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