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首页> 外文期刊>Nutrition and Cancer: An International Journal >Grape polyphenols inhibit Akt/mammalian target of rapamycin signaling and potentiate the effects of gefitinib in breast cancer
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Grape polyphenols inhibit Akt/mammalian target of rapamycin signaling and potentiate the effects of gefitinib in breast cancer

机译:葡萄多酚抑制雷帕霉素信号转导的Akt /哺乳动物靶点并增强吉非替尼在乳腺癌中的作用

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摘要

We recently reported that a combination of dietary grape polyphenols resveratrol, quercetin, and catechin (RQC), at low concentrations, was effective at inhibiting metastatic cancer progression. Herein, we investigate the molecular mechanisms of RQC in breast cancer and explore the potential of RQC as a potentiation agent for the epidermal growth factor receptor (EGFR) therapeutic gefitinib. Our in vitro experiments showed RQC induced apoptosis in gefitinib-resistant breast cancer cells via regulation of a myriad of proapoptotic proteins. Because the Akt/mammalian target of rapamycin (mTOR) signaling pathway is often elevated during development of anti-EGFR therapy resistance, the effect of RQC on the mTOR upstream effector Akt and the negative regulator AMP kinase (AMPK) was investigated. RQC was found to reduce Akt activity, induce the activation of AMPK, and inhibit mTOR signaling in breast cancer cells. Combined RQC and gefitinib decreased gefitinib resistant breast cancer cell viability to a greater extent than RQC or gefitinib alone. Moreover, RQC inhibited Akt and mTOR and activated AMPK even in the presence of gefitinib. Our in vivo experiments showed combined RQC and gefitinib was more effective than the individual treatments at inhibiting mammary tumor growth and metastasis in nude mice. Therefore, RQC treatment inhibits breast cancer progression and may potentiate anti-EGFR therapy by inhibition of Akt/mTOR signaling.
机译:我们最近报道,低浓度的饮食中的葡萄多酚白藜芦醇,槲皮素和儿茶素(RQC)的组合可有效抑制转移性癌症的进展。本文中,我们研究了RQC在乳腺癌中的分子机制,并探索了RQC作为表皮生长因子受体(EGFR)治疗性吉非替尼的增强剂的潜力。我们的体外实验表明,RQC通过调节多种促凋亡蛋白来诱导对吉非替尼耐药的乳腺癌细胞凋亡。由于在抗EGFR治疗耐药的发生过程中,雷帕霉素(mTOR)信号通路的Akt /哺乳动物靶标通常升高,因此研究了RQC对mTOR上游效应子Akt和负调节剂AMP激酶(AMPK)的影响。发现RQC降低了乳腺癌细胞中的Akt活性,诱导了AMPK的激活并抑制了mTOR信号传导。与单独的RQC或吉非替尼相比,RQC和吉非替尼联合使用在很大程度上降低了对吉非替尼耐药的乳腺癌细胞的生存能力。此外,即使存在吉非替尼,RQC也能抑制Akt和mTOR并激活AMPK。我们的体内实验表明,RQC和吉非替尼联合使用在抑制裸鼠乳腺肿瘤生长和转移方面比单独的治疗更为有效。因此,RQC治疗可抑制乳腺癌的进展,并可通过抑制Akt / mTOR信号传导来增强抗EGFR治疗。

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