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齿瓣石豆兰中具有抗肿瘤活性的吡咯里西啶生物碱通过自噬和凋亡的调节。

Pyrrolizidine alkaloids from Liparis nervosa with antitumor activity by modulation of autophagy and apoptosis.

机构信息

School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, Sichuan, PR China; School of Chemistry and Chemical Engineering, China West Normal University, Nanchong, 637002, Sichuan, PR China.

School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, Sichuan, PR China; Center for Molecular and Translational Medicine, Institute of Biomedical Sciences, Georgia State University, 511 Research Science Center, 157 Decatur St SE, Atlanta, GA, 30303, USA.

出版信息

Phytochemistry. 2018 Sep;153:147-155. doi: 10.1016/j.phytochem.2018.06.001. Epub 2018 Jun 29.

Abstract

Seven pyrrolizidine alkaloids, nervosine X-XV and nervosine VII N-oxide, together with a reaction product, namely chloride-(N-chloromethyl nervosine VII), were isolated from Liparis nervosa. Their structures were elucidated by extensive spectroscopic analyses. Most of these compounds were investigated for their cytotoxicity in vitro against HCT116 human cancer cell line, and the results showed that chloride-(N-chloromethyl nervosine VII) induced tumor cell death in a dose-dependent manner. Furthermore, the mechanisms underlying its cytotoxicity were investigated, including apoptosis and autophagy. Apoptosis in HCT116 cells was associated with up-regulation of caspase-3 and -9 expressions by activation of the mitochondrial pathway. The autophagy inducing effect was associated with the regulation of autophagic markers, including LC3-II, p62, and Beclin 1. Mechanistic studies showed that JNK, ERK1/2, and p38 MAPKs signaling cascades play an important role in chloride-(N-chloromethyl nervosine VII) induced autophagy and apoptosis.

摘要

从兰科石豆兰属植物密花石豆兰中分离得到 7 个吡咯里西啶生物碱,包括 nervosine X-XV 和 nervosine VII N-氧化物,以及一个反应产物,即氯化-(N-氯甲基 nervosine VII)。通过广泛的光谱分析阐明了它们的结构。对这些化合物进行了体外细胞毒性实验,检测它们对 HCT116 人癌细胞系的抑制活性,结果表明氯化-(N-氯甲基 nervosine VII)以剂量依赖的方式诱导肿瘤细胞死亡。此外,还研究了其诱导细胞毒性的机制,包括细胞凋亡和自噬。HCT116 细胞中的凋亡与 caspase-3 和 caspase-9 表达的上调有关,这是通过线粒体途径的激活引起的。自噬诱导作用与自噬标志物(包括 LC3-II、p62 和 Beclin 1)的调节有关。机制研究表明,JNK、ERK1/2 和 p38 MAPKs 信号级联在氯化-(N-氯甲基 nervosine VII)诱导的自噬和凋亡中发挥重要作用。

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