UCLA researchers in the Department of Obstetrics and Gynecology have discovered that ApoA-I can be used to treat and prevent pro-inflammatory skin conditions.
BACKGROUND
Inflammation is a standard immune signaling process that is strongly associated with stress and is connected to various diseases. Inflammation is activated to fight infection or invasion of potentially deleterious biological agents and to drive wound healing. While essential for these functions, inflammation can also exert detrimental effects. An unbalanced systemic inflammatory reaction can induce shock, derangement of microcirculation, and defects in coagulation. Antioxidants such as vitamin C, coffeeberry, and resveratrol have been used in the prevention and treatment of skin and systemic pro?inflammatory conditions.
Apolipoprotein A1 (ApoA?1) is the major protein component of HDL particles in the plasma. The protein, as a component of HDL particles, enables efflux of fat molecules by accepting fats from within cells for transport outside of the cells. ApoA?1 has been shown to have extremely strong and specific antioxidant activity.
INNOVATION
Researchers at UCLA have shown that ApoA?1 can significantly reduce the viability and proliferation of pro-inflammatory ID8 cells (mouse epithelial ovarian cancer cell line). An ApoA?1 mimetic (D?4f) was able to induce synthesis of mnSOD mRNA and protein, which inhibits cancer cell growth. To date, ApoA?1 has never been used for this purpose. However, the mechanism of action has already been determined, which will enable more directed development for therapeutic use.
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drive wound healing
exert detrimental effects
systemic pro‐inflammatory conditions
specific antioxidant activity
pro-inflammatory id8 cells