Suppr超能文献

可可多酚通过抑制鼠表皮细胞中磷酸肌醇 3-激酶(PI3K)和丝裂原活化蛋白激酶激酶-1(MEK1)的活性来抑制 TNF-α 诱导的血管内皮生长因子表达。

Cocoa polyphenols suppress TNF-α-induced vascular endothelial growth factor expression by inhibiting phosphoinositide 3-kinase (PI3K) and mitogen-activated protein kinase kinase-1 (MEK1) activities in mouse epidermal cells.

机构信息

Department of Agricultural Biotechnology, Seoul National University, Seoul, Republic of Korea.

出版信息

Br J Nutr. 2010 Oct;104(7):957-64. doi: 10.1017/S0007114510001704. Epub 2010 Jun 16.

Abstract

Cocoa polyphenols have antioxidant and anti-inflammatory effects. TNF-α is a pro-inflammatory cytokine that has a vital role in the pathogenesis of inflammatory diseases such as cancer and psoriasis. Vascular endothelial growth factor (VEGF) expression is associated with tumorigenesis, CVD, rheumatoid arthritis and psoriasis. We tested whether cocoa polyphenol extract (CPE) inhibited TNF-α-induced VEGF expression in promotion-sensitive JB6 mouse epidermal cells. CPE significantly inhibited TNF-α-induced up-regulation of VEGF via reducing TNF-α-induced activation of the nuclear transcription factors activator protein-1 (AP-1) and NF-κB, which are key regulators of VEGF expression. CPE also inhibited TNF-α-induced phosphorylation of protein kinase B (Akt) and extracellular signal-regulated kinase. CPE blocked activation of their downstream kinases, p70 kDa ribosomal protein S6 kinase and p90 kDa ribosomal protein S6 kinase. CPE suppressed phosphoinositide 3-kinase (PI3K) activity via binding PI3K directly. CPE did not affect TNF-α-induced phosphorylation of mitogen-activated protein kinase kinase-1 (MEK1) but suppressed TNF-α-induced MEK1 activity. Collectively, these results indicate that CPE reduced TNF-α-induced up-regulation of VEGF by directly inhibiting PI3K and MEK1 activities, which may contribute to its chemopreventive potential.

摘要

可可多酚具有抗氧化和抗炎作用。TNF-α 是一种促炎细胞因子,在癌症和银屑病等炎症性疾病的发病机制中起着至关重要的作用。血管内皮生长因子(VEGF)的表达与肿瘤发生、CVD、类风湿关节炎和银屑病有关。我们测试了可可多酚提取物(CPE)是否抑制 TNF-α 诱导的促癌敏感 JB6 小鼠表皮细胞中 VEGF 的表达。CPE 通过减少 TNF-α 诱导的核转录因子激活蛋白-1(AP-1)和 NF-κB 的激活,显著抑制 TNF-α 诱导的 VEGF 上调,AP-1 和 NF-κB 是 VEGF 表达的关键调节剂。CPE 还抑制了 TNF-α 诱导的蛋白激酶 B(Akt)和细胞外信号调节激酶的磷酸化。CPE 阻断了其下游激酶 p70 核糖体蛋白 S6 激酶和 p90 核糖体蛋白 S6 激酶的激活。CPE 通过直接结合 PI3K 抑制磷酸肌醇 3-激酶(PI3K)的活性。CPE 不影响 TNF-α 诱导的丝裂原激活蛋白激酶激酶-1(MEK1)的磷酸化,但抑制 TNF-α 诱导的 MEK1 活性。综上所述,这些结果表明,CPE 通过直接抑制 PI3K 和 MEK1 的活性来减少 TNF-α 诱导的 VEGF 上调,这可能有助于其化学预防潜力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验