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The Role of Ferroptosis in Cancer Development and Treatment Response

Ferroptosis is a process driven by accumulated iron-dependent lipid ROS that leads to cell death, which is a distinct regulated cell death comparing to other cell death. The lethal metabolic imbalance resulted from GSH depletion or inactivation of glutathione peroxidase 4 is the executor of ferropto...

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Autores principales: Lu, Bin, Chen, Xiao Bing, Ying, Mei Dan, He, Qiao Jun, Cao, Ji, Yang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770584/
https://www.ncbi.nlm.nih.gov/pubmed/29375387
http://dx.doi.org/10.3389/fphar.2017.00992
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author Lu, Bin
Chen, Xiao Bing
Ying, Mei Dan
He, Qiao Jun
Cao, Ji
Yang, Bo
author_facet Lu, Bin
Chen, Xiao Bing
Ying, Mei Dan
He, Qiao Jun
Cao, Ji
Yang, Bo
author_sort Lu, Bin
collection PubMed
description Ferroptosis is a process driven by accumulated iron-dependent lipid ROS that leads to cell death, which is a distinct regulated cell death comparing to other cell death. The lethal metabolic imbalance resulted from GSH depletion or inactivation of glutathione peroxidase 4 is the executor of ferroptosis within the cancer cell. Small molecules-induced ferroptosis has a strong inhibition of tumor growth and enhances the sensitivity of chemotherapeutic drugs, especially in the condition of drug resistance. These evidences have highlighted the importance of ferroptosis in cancer therapeutics, but the roles of ferroptosis in tumorigenesis and development remain unclear. This article provides an overview of the mechanisms of ferroptosis, highlights the role of ferroptosis in cancer and discusses strategies for therapeutic modulation.
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spelling pubmed-57705842018-01-26 The Role of Ferroptosis in Cancer Development and Treatment Response Lu, Bin Chen, Xiao Bing Ying, Mei Dan He, Qiao Jun Cao, Ji Yang, Bo Front Pharmacol Pharmacology Ferroptosis is a process driven by accumulated iron-dependent lipid ROS that leads to cell death, which is a distinct regulated cell death comparing to other cell death. The lethal metabolic imbalance resulted from GSH depletion or inactivation of glutathione peroxidase 4 is the executor of ferroptosis within the cancer cell. Small molecules-induced ferroptosis has a strong inhibition of tumor growth and enhances the sensitivity of chemotherapeutic drugs, especially in the condition of drug resistance. These evidences have highlighted the importance of ferroptosis in cancer therapeutics, but the roles of ferroptosis in tumorigenesis and development remain unclear. This article provides an overview of the mechanisms of ferroptosis, highlights the role of ferroptosis in cancer and discusses strategies for therapeutic modulation. Frontiers Media S.A. 2018-01-12 /pmc/articles/PMC5770584/ /pubmed/29375387 http://dx.doi.org/10.3389/fphar.2017.00992 Text en Copyright © 2018 Lu, Chen, Ying, He, Cao and Yang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Lu, Bin
Chen, Xiao Bing
Ying, Mei Dan
He, Qiao Jun
Cao, Ji
Yang, Bo
The Role of Ferroptosis in Cancer Development and Treatment Response
title The Role of Ferroptosis in Cancer Development and Treatment Response
title_full The Role of Ferroptosis in Cancer Development and Treatment Response
title_fullStr The Role of Ferroptosis in Cancer Development and Treatment Response
title_full_unstemmed The Role of Ferroptosis in Cancer Development and Treatment Response
title_short The Role of Ferroptosis in Cancer Development and Treatment Response
title_sort role of ferroptosis in cancer development and treatment response
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770584/
https://www.ncbi.nlm.nih.gov/pubmed/29375387
http://dx.doi.org/10.3389/fphar.2017.00992
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