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"Oxidative stress pathway proteins" refers to a heterogeneous collection of enzymes, transcription factors, chaperones, and signaling mediators that either generate, sense, detoxify, or transduce the cellular effects of reactive oxygen species (ROS) and related redox imbalances. Examples include antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase), transcription factors regulating oxidative stress response (NRF2, OxyR), and molecular chaperones (heat shock proteins). These proteins are fundamental for maintaining redox homeostasis, modulating apoptosis and inflammation, and their dysregulation is implicated in a variety of diseases including cancer, cardiovascular disease, neurodegenerative disorders, and aging. They are not a discrete drug target but represent a category of functionally related proteins relevant to many therapeutic strategies[4][5][6][8].
Antioxidant activity (scavenging ROS); Induction of antioxidant protein expression (e.g., NRF2 activators); Inhibition of oxidative enzymes (e.g., NOX inhibitors); Modulation of signaling pathways related to stress response (e.g., MAPK, NF-κB, KEAP1-NRF2-ARE)
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