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Title: Epigenetic modifications of triterpenoid ursolic acid in activating Nrf2 and blocking cellular transformation of mouse epidermal cells.

Authors: Kim, Hyuck; Ramirez, Christina N; Su, Zheng-Yuan; Kong, Ah-Ng Tony

Published In J Nutr Biochem, (2016 07)

Abstract: Ursolic acid (UA), a well-known natural triterpenoid found in abundance in blueberries, cranberries and apple peels, has been reported to possess many beneficial health effects. These effects include anticancer activity in various cancers, such as skin cancer. Skin cancer is the most common cancer in the world. Nuclear factor E2-related factor 2 (Nrf2) is a master regulator of antioxidative stress response with anticarcinogenic activity against UV- and chemical-induced tumor formation in the skin. Recent studies show that epigenetic modifications of Nrf2 play an important role in cancer prevention. However, the epigenetic impact of UA on Nrf2 signaling remains poorly understood in skin cancer. In this study, we investigated the epigenetic effects of UA on mouse epidermal JB6 P+ cells. UA inhibited cellular transformation by 12-O-tetradecanoylphorbol-13-acetate at a concentration at which the cytotoxicity was no more than 25%. Under this condition, UA induced the expression of the Nrf2-mediated detoxifying/antioxidant enzymes heme oxygenase-1, NAD(P)H:quinone oxidoreductase 1 and UDP-glucuronosyltransferase 1A1. DNA methylation analysis revealed that UA demethylated the first 15 CpG sites of the Nrf2 promoter region, which correlated with the reexpression of Nrf2. Furthermore, UA reduced the expression of epigenetic modifying enzymes, including the DNA methyltransferases DNMT1 and DNMT3a and the histone deacetylases (HDACs) HDAC1, HDAC2, HDAC3 and HDAC8 (Class I) and HDAC6 and HDAC7 (Class II), and HDAC activity. Taken together, these results suggest that the epigenetic effects of the triterpenoid UA could potentially contribute to its beneficial effects, including the prevention of skin cancer.

PubMed ID: 27260468 Exiting the NIEHS site

MeSH Terms: Animals; Anticarcinogenic Agents/adverse effects; Anticarcinogenic Agents/metabolism*; Antioxidants/adverse effects; Antioxidants/metabolism; Carcinogens/antagonists & inhibitors; Carcinogens/toxicity; Cell Line; Cell Survival/drug effects; Cell Transformation, Neoplastic*/drug effects; DNA (Cytosine-5-)-Methyltransferases/chemistry; DNA (Cytosine-5-)-Methyltransferases/genetics; DNA (Cytosine-5-)-Methyltransferases/metabolism; DNA Methylation/drug effects; Dietary Supplements/adverse effects; Enzyme Repression/drug effects; Epidermal Cells; Epidermis/drug effects; Epidermis/metabolism*; Epigenesis, Genetic*/drug effects; Histone Deacetylases/chemistry; Histone Deacetylases/genetics; Histone Deacetylases/metabolism; Mice; NF-E2-Related Factor 2/agonists*; NF-E2-Related Factor 2/genetics; NF-E2-Related Factor 2/metabolism; Oxidative Stress/drug effects; Promoter Regions, Genetic/drug effects; Skin Neoplasms/chemically induced; Skin Neoplasms/metabolism; Skin Neoplasms/prevention & control*; Triterpenes/adverse effects; Triterpenes/metabolism*

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