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The glutathione system is a fundamental cellular defense network comprising the tripeptide glutathione (GSH) and several key enzymes, including glutathione peroxidases (GPx), glutathione reductases (GR), and glutathione S-transferases (GST) [2, 6, 23]. Its primary role is maintaining cellular redox homeostasis by neutralizing reactive oxygen species and detoxifying a wide range of endogenous and exogenous electrophiles through Phase II conjugation [2, 7, 23]. In oncology, the system is frequently exploited by tumor cells, which overexpress GSTs to deactivate chemotherapeutic drugs, leading to multi-drug resistance [1, 12, 13]. Conversely, a deficiency in the glutathione system is linked to neurodegenerative diseases, chronic inflammation, and viral infections, where oxidative stress predominates [6, 9, 11]. Therapeutic interventions include the use of GSH precursors like N-acetylcysteine to replenish cellular stores, GST inhibitors like ethacrynic acid to sensitize cancer cells, and Nrf2 activators to enhance the overall antioxidant response [1, 9, 11, 12]. However, targeting this system carries risks, as profound GSH depletion can trigger severe organ damage, and exogenous administration has been linked to rare but serious adverse reactions like anaphylaxis [14, 15, 16].
Modulation of cellular redox state and detoxification capacity through enzyme inhibition (e.g., GST, GCL), substrate supplementation (e.g., NAC, GSH), or transcriptional activation of the Nrf2 pathway [1, 9, 11, 12, 23].
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