Ferroptosis, a new type of cell death, is the iron dependent form of nonaptotic cell death triggered by the oncogenic RAS-selective lethal small molecule erastin (Nonapoptotic forms of cell death may facilitate the selective elimination of some tumor cells or be activated in specific pathological states). Ferroptosis is dependent upon intracellular iron, but not other metals, and is morphologically, biochemically, and genetically distinct from
apoptosis, necrosis, and autophagy. Erastin inhibits cystine uptake by the cystine/glutamate antiporter, creating a void in the antioxidant defenses of the cell and ultimately leading to iron-dependent, oxidative death. Thus, activation of ferroptosis results in the nonapoptotic destruction of certain cancer cells.
apoptosis, necrosis, and autophagy. Erastin inhibits cystine uptake by the cystine/glutamate antiporter, creating a void in the antioxidant defenses of the cell and ultimately leading to iron-dependent, oxidative death. Thus, activation of ferroptosis results in the nonapoptotic destruction of certain cancer cells.
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