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ATF4 in cellular stress, ferroptosis, and cancer.

Authors :
Tang, Hu
Kang, Rui
Liu, Jiao
Tang, Daolin
Source :
Archives of Toxicology. Apr2024, Vol. 98 Issue 4, p1025-1041. 17p.
Publication Year :
2024

Abstract

Activating transcription factor 4 (ATF4), a member of the ATF/cAMP response element-binding (CREB) family, plays a critical role as a stress-induced transcription factor. It orchestrates cellular responses, particularly in the management of endoplasmic reticulum stress, amino acid deprivation, and oxidative challenges. ATF4's primary function lies in regulating gene expression to ensure cell survival during stressful conditions. However, when considering its involvement in ferroptosis, characterized by severe lipid peroxidation and pronounced endoplasmic reticulum stress, the ATF4 pathway can either inhibit or promote ferroptosis. This intricate relationship underscores the complexity of cellular responses to varying stress levels. Understanding the connections between ATF4, ferroptosis, and endoplasmic reticulum stress holds promise for innovative cancer therapies, especially in addressing apoptosis-resistant cells. In this review, we provide an overview of ATF4, including its structure, modifications, and functions, and delve into its dual role in both ferroptosis and cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03405761
Volume :
98
Issue :
4
Database :
Academic Search Index
Journal :
Archives of Toxicology
Publication Type :
Academic Journal
Accession number :
176083081
Full Text :
https://doi.org/10.1007/s00204-024-03681-x