To explore the role of PPARa in regulating FSP1 in vivo, we established PPARa over-expression and knockdown models in mice by intraspinal injection of lentivirus (Fig S3b, c)
In ferroptosis, p53 transcriptionally represses SLC7A11, thereby curtailing GSH synthesis and sensitizing cells to this form of death ( 4.5 Synergistic versus antagonistic potential These mechanistic overlaps provide a compelling rationale for a combinatorial therapeutic assault
Here, we first summarize the canonical CoQ 10 biosynthetic pathway and provide a comprehensive overview of both established and emerging CoQ 10 oxidoreductases, such as FSP1, DHODH, SQOR and additional enzymes, emphasizing their biochemical roles in ferroptosis regulation
This dichotomy suggests that histone crotonylation plays a dual role at different stages post-MI, indicating that specific crotonylation sites may represent potential therapeutic targets for cardiac hypertrophy