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R Cytosolic GSTs function as homodimers or heterodimers with a conserved N-terminal domain containing the GSH binding site (G-site) and a variable C-terminal domain containing the hydrophobic substrate binding site (H-site)

Importantly, combining mTORC1 inhibitors with imidazole ketone erastin (IKE), a bioavailable ferroptosis inducer, exhibited synergistic tumor-suppressing effects in patient-derived xenografts of lung cancer

Remarkably, Nrf2 knockdown reduced QCTs protective effects against ferroptosis, emphasizing its crucial role in QCTs neuroprotective actions