COMPOSITIONS AND METHODS FOR INHIBITING FSP1
Researchers at UC Berkeley have developed ferroptosis suppressor protein 1 (FSP1) inhibitors and methods for their use in cancer therapy.
Ferroptosis is an iron-dependent, non-apoptotic form of regulated cell death that is characterized by the accumulation of oxidatively damaged phospholipids. Ferroptosis has been implicated in cell death and dysfunction in degenerative diseases. Triggering ferroptosis by inhibition of the GSH-GPX4 pathway has emerged as a promising strategy to trigger cell death in cancer. However, recent findings have uncovered protective mechanisms that promote resistance to ferroptosis inducing agents in cancer cells. For example, FSP1 mediates a GSH-independent ferroptosis suppression pathway and has emerged as a key ferroptosis resistance factor. Thus, a need exists for FSP1 inhibitors and their use in cancer therapy.
Stage of Research
The inventors have developed FSP1 inhibitors and methods of inhibiting FSP1 comprised of contacting FSP1 with an FSP1 inhibitor in an amount effective to inhibit FSP1. The inventors have also developed methods for treating cancer wherein a subject is treated with a therapeutically effective amount of an FSP1 inhibitor, sometimes in a combination therapy regime.
Applications
Advantages
Stage of Development
Research – in vitro
Publications
Identification of structurally diverse FSP1 inhibitors that sensitize cancer cells to ferroptosis. Hendricks, J.M., Olzmann, J.A., et al., Cell Chemical Biology. (2023) 4;S2451-9456(23)00114-9.
Related Web Links
https://www.olzmannlab.com/
Keywords
Ferroptosis, FSP1, cancer
Technology Reference
Biohub ref. no. CZB-237B
Berkeley ref. no. B22-061