(-)-epigallocatechin gallate induces Nrf2-mediated antioxidant enzyme expression via activation of PI3K and ERK in human mammary epithelial cells

被引:246
|
作者
Na, Hye-Kyung [1 ]
Kim, Eun-Hee [1 ]
Jung, Joo-Hee [1 ]
Lee, Hyun-Hee [1 ]
Hyun, Jin-Won [2 ,3 ]
Surh, Young-Joon [1 ,4 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South Korea
[2] Jeju Natl Univ, Coll Med, Dept Biochem, Cheju 690756, South Korea
[3] Jeju Natl Univ, Appl Radiol Sci Res Inst, Cheju 690756, South Korea
[4] Seoul Natl Univ, Canc Res Inst, Seoul 110799, South Korea
关键词
antioxidant enzymes; EGCG; Nrf2; manganese superoxide dismutase; glutamate-cysteine ligase; heme oxygenase; MCF10A cells;
D O I
10.1016/j.abb.2008.04.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The chemopreventive and chemoprotective activities of green tea have been attributed to the polyphenolic ingredient (-)-epigallocatechin-3-gallate (EGCG). Here, we report that treatment of human breast epithelial (MCF10A) cells with EGCG induces the expression of glutamate-cysteine ligase, manganese superoxide dismutase (MnSOD), and heme oxygenase-1 (HO-1). NF-E2-related factor (Nrf2) has been reported to regulate the antioxidant response element (ARE)-mediated expression of many antioxidant as well as detoxifying enzymes. The nuclear accumulation, ARE binding and transcriptional activity of Nrf2 were increased by EGCG treatment. Silencing of Nrf2 by siRNA gene knockdown rendered the MCF10A cells less sensitive to the EGCG-induced expression of HO-1 and MnSOD. Furthermore, EGCG activated Akt and extracellular signal-regulated protein kinase1/2 (ERK1/2). The pharmacologic inhibition of these kinases abrogated the nuclear translocation of Nrf2 induced by EGCG. These findings suggest that Nrf2 mediates EGCG-induced expression of some representative antioxidant enzymes, possibly via Akt and ERK1/2 signaling, which may provide the cells with acquired antioxidant defense capacity to survive the oxidative stress. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:171 / 177
页数:7
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