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To evaluate the sensitivity of the two culture systems to ferroptotic cell death, we treated the four lung cancer primary cultures (BBIRE-T248, PUC30, PUC36, and PUC37) with RSL3, a ferroptosis activator with selectivity for tumor cells bearing oncogenic Ras, which acts by inhibiting the glutathione peroxidase 4 (GPX4)

GHK-Cu drives VEGF through direct fibroblast stimulation and copper-dependent enzymatic activity

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