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温州蜜柑果皮诱导人乳腺癌MCF-7细胞凋亡:与活性氧依赖的AMPK激活有关

Induction of Apoptosis by Citrus unshiu Peel in Human Breast Cancer MCF-7 Cells: Involvement of ROS-Dependent Activation of AMPK.

作者信息

Kim Min Yeong, Bo Hyun Hwang, Choi Eun Ok, Kwon Da He, Kim Hong Jae, Ahn Kyu Im, Ji Seon Yeong, Jeong Jin-Woo, Park Shin-Hyung, Hong Su-Hyun, Kim Gi-Young, Park Cheol, Kim Heui-Soo, Moon Sung-Kwon, Yun Seok-Joong, Kim Wun Jae, Choi Yung Hyun

机构信息

Department of Biochemistry, Dongeui University College of Korean Medicine.

Anti-Aging Research Center, Dongeui University.

出版信息

Biol Pharm Bull. 2018;41(5):713-721. doi: 10.1248/bpb.b17-00898.

Abstract

The fruit of Citrus unshiu MARKOVICH used for various purposes in traditional medicine has various pharmacological properties including antioxidant, anti-inflammatory, and antibacterial effects. Recently, the possibility of anti-cancer activity of the extracts or components of this fruit has been reported; however, the exact mechanism has not yet been fully understood. In this study, we evaluated the anti-proliferative effect of water extract of C. unshiu peel (WECU) on human breast cancer MCF-7 cells and investigated the underlying mechanism. Our results showed that reduction of MCF-7 cell survival by WECU was associated with the induction of apoptosis. WECU-induced apoptotic cell death was related to the activation of caspase-8 and -9, representative initiate caspases of extrinsic and intrinsic apoptosis pathways, respectively, and increase in the Bax : Bcl-2 ratio accompanied by cleavage of poly(ADP-ribose) polymerase (PARP). WECU also increased the mitochondrial dysfunction and cytosolic release of cytochrome c. In addition, AMP-activated protein kinase (AMPK) and its downstream target molecule, acetyl-CoA carboxylase, were activated in a concentration-dependent manner in WECU-treated cells. In contrast, compound C, an AMPK inhibitor, significantly inhibited WECU-induced apoptosis, while inhibiting increased expression of Bax and decreased expression of Bcl-2 by WECU and inhibition of WECU-induced PARP degradation. Furthermore, WECU provoked the production of reactive oxygen species (ROS); however, the activation of AMKP and apoptosis by WECU were prevented, when the ROS production was blocked by antioxidant N-acetyl cysteine. Therefore, our data indicate that WECU suppresses MCF-7 cell proliferation by activating the intrinsic and extrinsic apoptosis pathways through ROS-dependent AMPK pathway activation.

摘要

传统医学中,温州蜜柑(Citrus unshiu MARKOVICH)的果实被用于多种用途,具有多种药理特性,包括抗氧化、抗炎和抗菌作用。最近,有报道称该果实的提取物或成分具有抗癌活性;然而,确切机制尚未完全明确。在本研究中,我们评估了温州蜜柑果皮水提取物(WECU)对人乳腺癌MCF-7细胞的抗增殖作用,并研究了其潜在机制。我们的结果表明,WECU降低MCF-7细胞存活率与诱导细胞凋亡有关。WECU诱导的凋亡细胞死亡分别与凋亡外源性和内源性途径的代表性起始半胱天冬酶caspase-8和-9的激活有关,同时伴随着聚(ADP-核糖)聚合酶(PARP)的裂解,Bax : Bcl-2比值增加。WECU还增加了线粒体功能障碍和细胞色素c的胞质释放。此外,在WECU处理的细胞中,AMP激活的蛋白激酶(AMPK)及其下游靶分子乙酰辅酶A羧化酶以浓度依赖性方式被激活。相反,AMPK抑制剂化合物C显著抑制WECU诱导的细胞凋亡,同时抑制WECU诱导的Bax表达增加和Bcl-2表达降低以及WECU诱导的PARP降解。此外,WECU引发了活性氧(ROS)的产生;然而,当抗氧化剂N-乙酰半胱氨酸阻断ROS产生时,WECU对AMKP的激活和细胞凋亡被阻止。因此,我们的数据表明,WECU通过ROS依赖性AMPK途径激活,激活内源性和外源性凋亡途径,从而抑制MCF-7细胞增殖。

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