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Flavokawain B 的体外和体内抗血管生成作用。

The In Vitro and In Vivo Antiangiogenic Effects of Flavokawain B.

机构信息

Department of Surgery, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Department of Mental Health, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

出版信息

Phytother Res. 2017 Oct;31(10):1607-1613. doi: 10.1002/ptr.5891. Epub 2017 Aug 17.

DOI:10.1002/ptr.5891
PMID:28816367
Abstract

Angiogenesis is implicated in the development of a variety of pathological processes, most commonly cancer. It is essential for tumor growth and metastasis, making it an important cancer therapeutic target. Naturally occurring substances have led to the discovery of anticancer agents. Flavokawain B (FKB), a chalcone isolated from the root extracts of kava-kava plant, inhibits proliferation and causes apoptosis in vitro and in vivo of various cancer cell lines. The antimetastatic potential of FKB has also been suggested. In our study, we confirm the antiangiogenic action of FKB in vitro and, for the first time, demonstrate its strong antiangiogenic activity in vivo, using a zebrafish model. Our data show that FKB inhibits human brain endothelial cell (HUVEC) migration and tube formation even at very low and non-toxic concentrations. Moreover, FKB blocks angiogenesis process in zebrafish, with a dramatic reduction of subintestinal vein formation in a dose-dependent manner. Flavokawain B at the concentration of 2.5 μg/mL did not exhibit any toxic effects in zebrafish larvae and caused a markedly or complete obliteration of subintestinal vein formation. Our findings along with previously published data confirm that FKB may form the basis for creating an additional tool in the treatment of cancer and other neovascularization-related diseases. Copyright © 2017 John Wiley & Sons, Ltd.

摘要

血管生成与多种病理过程的发展有关,最常见的是癌症。它对肿瘤的生长和转移至关重要,使其成为癌症治疗的重要靶点。天然存在的物质导致了抗癌药物的发现。Flavokawain B(FKB)是从卡瓦植物根提取物中分离出的一种查耳酮,可抑制多种癌细胞系的体外和体内增殖并诱导细胞凋亡。还提示了 FKB 的抗转移潜力。在我们的研究中,我们在体外证实了 FKB 的抗血管生成作用,并且首次在斑马鱼模型中证明了其在体内的强烈抗血管生成活性。我们的数据表明,FKB 甚至在非常低且无毒的浓度下也能抑制人脑血管内皮细胞(HUVEC)的迁移和管状形成。此外,FKB 可阻断斑马鱼的血管生成过程,以剂量依赖性方式显着减少次级肠静脉的形成。浓度为 2.5μg/mL 的 Flavokawain B 在斑马鱼幼虫中没有表现出任何毒性作用,并导致次级肠静脉形成明显或完全消失。我们的发现以及先前发表的数据证实,FKB 可能为治疗癌症和其他血管新生相关疾病提供新的治疗方法。版权所有©2017 John Wiley & Sons, Ltd.

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