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In addition to direct effects on hepatic lipid synthesis, LXR repression exerts pleiotropic effects to reduce dyslipidemia

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[3] Additionally, glycine itself appears to have direct insulin-sensitizing properties: it stimulates glucagon-like peptide-1 (GLP-1) secretion from intestinal L-cells, activates hepatic GLP-1 receptors, and modulates bile acid composition in ways that favor improved glucose homeostasis

A recent study has shown that Yap is associated with the activation of ferroptosis, Yap can promote an iron environment in cancer cells through stimulating transcription of TEAF-based members of the Transferrin receptor (TFRC) and Acyl-CoA synthetase long chain family 4 (ACSL4) [129, 130]

Inflammation-driven senescence-associated secretory phenotype in cancer-associated fibroblasts enhances peritoneal dissemination