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GPX4-AUTAC induces ferroptosis in breast cancer by promoting the selective autophagic degradation of GPX4 mediated by TRAF6-p62

Cell Death & Differentiation
Emerging evidence indicates that activation of ferroptosis by inhibition of glutathione peroxidase 4 (GPX4) may be exploited as a therapeutic strategy to suppress tumor growth and progression. However, application of GPX4 inhibitors in cancer treatment is hampered by their poor selectivity, which results in unfavorable toxicity.
Rong Gong   +13 more
openaire   +2 more sources

An overview of GPX4-targeting TPDs for cancer therapy

Bioorganic & Medicinal Chemistry
Ferroptosis is a newly identified form of regulated, non-apoptotic cell death caused by iron-dependent phospholipid peroxidation. Glutathione peroxidase 4 (GPX4) inactivation-induced ferroptosis is an efficient antitumor treatment. Currently, several GPX4 inhibitors have been identified.
Xiaojuan, Yang   +2 more
openaire   +2 more sources

Interfering with GPX4 degradation

Nature Chemical Biology
Jing Li, Yuhan Zhou, Weimin Wang
openaire   +2 more sources

GPX4 methylation puts a brake on ferroptosis

Nature Cell Biology
Graeme I. Lancaster, Andrew J. Murphy
openaire   +2 more sources

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