Acsl4 Dictates Ferroptosis Sensitivity by Shaping Cellular Lipid Composition

Explore this paper's citation graph

Summary

It is demonstrated that pharmacological targeting of Acsl4 with the antidiabetic compound class, thiazolidinediones, ameliorates tissue demise in a murine model of ferroptosis, suggesting that Acsl4 inhibition is a viable therapeutic approach to prevent ferroptosis-related diseases.

Type
article
Published
2016-11-14
Cited by
3,715
References
54
Access
Open access

Keywords

GPX4, Biology, Programmed cell death, Cell biology, Chemistry

References

Cited by

Related papers