Jiang Jin-Huan, Pi Jiang, Jin Hua, Yang Fen, Cai Ji-Ye
State Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China.
State Key Laboratory of Quality Research in Chinese Medicines, Macau University of Science and Technology, Macau, China; Department of Chemistry, Jinan University, GuangZhou, China.
Pathol Res Pract. 2018 May;214(5):691-699. doi: 10.1016/j.prp.2018.03.015. Epub 2018 Mar 15.
Matrine, as a natural alkaloid isolated from the traditional herb medicine sophora flavescens, has been proved to possess excellent biological activities, including anticancer effects. Now, this research aims to assess the anticancer activities and the mechanism of matrine against esophageal cancer cells, we investigated the proliferative inhibition, apoptosis induction, as well as the underlying mechanism of matrine on esophageal cancer KYSE-150 cells. It was found that matrine could suppress KYSE-150 cell proliferation and significantly mediate cell apoptosis in a dose-dependent relation by increasing intracellular reactive oxygen species level and triggering mitochondrial membrane potential disruption. More precise mechanism studies demonstrated that matrine could up-regulate the expression of Bax proteins and down-regulate the expression of Bcl-2 proteins, as well as the activation about caspase-3, 8 and 9 in KYSE-150 cells. The morphological analysis of KYSE-150 cells exhibited that matrine could destroy the F-actin and nuclei structures and induce morphological damage with increased surface height distribution and roughness of cell membrane. These results not only demonstrated the potential anticancer activity mechanism of matrine at nanoscale, but also provide preliminary guidance for the treatment of esophageal cancer using matrine.
苦参碱作为从传统草药苦参中分离出的一种天然生物碱,已被证明具有出色的生物活性,包括抗癌作用。目前,本研究旨在评估苦参碱对食管癌细胞的抗癌活性及其作用机制,我们研究了苦参碱对食管癌KYSE-150细胞的增殖抑制、凋亡诱导作用及其潜在机制。研究发现,苦参碱可抑制KYSE-150细胞增殖,并通过增加细胞内活性氧水平和引发线粒体膜电位破坏,以剂量依赖的方式显著介导细胞凋亡。更精确的机制研究表明,苦参碱可上调KYSE-150细胞中Bax蛋白的表达,下调Bcl-2蛋白的表达,并激活caspase-3、8和9。KYSE-150细胞的形态分析表明,苦参碱可破坏F-肌动蛋白和细胞核结构,并诱导形态损伤,同时细胞膜表面高度分布和粗糙度增加。这些结果不仅揭示了苦参碱在纳米尺度上潜在的抗癌活性机制,也为苦参碱治疗食管癌提供了初步指导。