Journal article

Caspase-2 protects against ferroptotic cell death

Swati Dawar, Mariana C Benitez, Yoon Lim, Toby A Dite, Jumana M Yousef, Niko Thio, Sylvain Garciaz, Thomas D Jackson, Julia V Milne, Laura F Dagley, Wayne A Phillips, Sharad Kumar, Nicholas J Clemons

Cell Death and Disease | Nature Publishing Group | Published : 2024

Abstract

Caspase-2, one of the most evolutionarily conserved members of the caspase family, is an important regulator of the cellular response to oxidative stress. Given that ferroptosis is suppressed by antioxidant defense pathways, such as that involving selenoenzyme glutathione peroxidase 4 (GPX4), we hypothesized that caspase-2 may play a role in regulating ferroptosis. This study provides the first demonstration of an important and unprecedented function of caspase-2 in protecting cancer cells from undergoing ferroptotic cell death. Specifically, we show that depletion of caspase-2 leads to the downregulation of stress response genes including SESN2, HMOX1, SLC7A11, and sensitizes mutant-p53 can..

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Grants

Funding Acknowledgements

We thank all the members of our laboratory for their discussions and useful comments. Specifically, we thank Karen Montgomery for help with dose-response experiments, and Metta Jenna from the Center for Advanced Histology and Microscopy core facility within Peter Mac, for help with live-cell imaging. Lastly, we thank GenScript for generating caspase-2 mutant constructs and the BirA*-Casp2C320G construct.