Additionally, around 12% of oxygen used in mitochondrial metabolism produces free radicals, which can lead to oxidative stress and even DNA damage [2]
Wang J, Liu Y, Zhou LJ, Wu Y, Li F, Shen KF,
Water, Cyclopentasiloxane, Zinc Oxide (CI 77947), Ethylhexyl Methoxycinnamate, Titanium Dioxide (CI 77891), Cyclohexasiloxane, Ethylhexyl Salicylate, Octocrylene, Butylene Glycol, Diphenylsiloxy Phenyl Trimethicone, Dipropylene Glycol, Niacinamide, Phenyl Trimethicone, Lauryl Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Arbutin, Sorbitan Isostearate, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Tangerina (Tangerine) Extract (300ppb), Polymethyl Methacrylate, Polymethylsilsesquioxane, Disteardimonium Hectorite, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Aluminum Hydroxide, Magnesium Sulfate, Stearic Acid, Cetearyl Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Caprylyl Glycol, Hydroxyacetophenone, Adenosine, Sodium Ascorbyl Phosphate (100ppb), 1,2-Hexanediol, Acrylates Copolymer, Ethylhexylglycerin, Disodium EDTA, Limonene, Linalool
Recent elegant work has definitively identified that TP53 missense mutations in myeloid malignancies result in a dominant-negative effect without evidence of neomorphic gain-of-function activities, ultimately leading to a selection advantage when exposed to DNA damage.12 Thus, restoring wild-type function in TP53 mutant clones would be of profound beneficial impact
