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Updated: Sep 5, 2026

Revealing the Ferroptotic Phenotype of Medulloblastoma
Published on: March 15, 2024
Metabolite buffering of labile iron governs ferroptosis
Amalia H Megarioti1, James A Olzmann1
1Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA; Department of Metabolic Biology and Nutrition, University of California, Berkeley, Berkeley, CA 94720, USA.
Abstract:
Iron abundance alone does not determine ferroptosis sensitivity. In this issue of Cell, Sharma and colleagues identify polyamines as endogenous metabolic buffers that reduce the chemical accessibility of labile iron, revealing an unexpected function for one of the cell's most abundant metabolite classes while raising new questions about the organization of intracellular iron metabolism.
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