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Ferroptosis: A flexible constellation of related biochemical mechanisms.
Dixon, Scott J; Pratt, Derek A.
  • Dixon SJ; Department of Biology, Stanford University, Stanford, CA, USA. Electronic address: sjdixon@stanford.edu.
  • Pratt DA; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, ON, Canada. Electronic address: dpratt@uottawa.ca.
Mol Cell ; 83(7): 1030-1042, 2023 04 06.
Article en En | MEDLINE | ID: mdl-36977413
ABSTRACT
It is common to think about and depict biological processes as being governed by fixed pathways with specific components interconnected by concrete positive and negative interactions. However, these models may fail to effectively capture the regulation of cell biological processes that are driven by chemical mechanisms that do not rely absolutely on specific metabolites or proteins. Here, we discuss how ferroptosis, a non-apoptotic cell death mechanism with emerging links to disease, may be best understood as a highly flexible mechanism that can be executed and regulated by many functionally related metabolites and proteins. The inherent plasticity of ferroptosis has implications for how to define and study this mechanism in healthy and diseased cells and organisms.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ferroptosis Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ferroptosis Idioma: En Año: 2023 Tipo del documento: Article