首页> 外文期刊>Pathology Research and Practice >Chinese herb medicine matrine induce apoptosis in human esophageal squamous cancer KYSE-150 cells through increasing reactive oxygen species and inhibiting mitochondrial function
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Chinese herb medicine matrine induce apoptosis in human esophageal squamous cancer KYSE-150 cells through increasing reactive oxygen species and inhibiting mitochondrial function

机译:中草药医学苦参碱通过增加反应性氧物种和抑制线粒体功能,诱导人食管鳞癌Kyse-150细胞的细胞凋亡

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摘要

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.
机译:作为从传统的草药Sophora Flavescens分离的天然生物碱的苦参碱已被证明具有优异的生物活性,包括抗癌效果。现在,该研究旨在评估抗癌活动和苦参碱对食管癌细胞的机制,我们研究了增殖性抑制,凋亡诱导,以及苦参碱对食管癌Kyse-150细胞的潜在机制。结果发现,通过增加细胞内反应性氧物质水平并引发线粒体膜潜在破坏,苦参碱可以抑制Kyse-150细胞增殖并显着介导细胞凋亡。更精确的机制研究表明,苦参碱可以上调Bax蛋白的表达和下调Bcl-2蛋白的表达,以及Kyse-150细胞中的Caspase-3,8和9的活化。 Kyse-150细胞的形态学分析表明,苦参碱可以破坏F型肌动蛋白和核结构,并用增加的表面高度分布和细胞膜的粗糙度诱导形态损伤。这些结果不仅证明了纳米级菌核的潜在抗癌活性机制,而且还提供了使用苦参碱治疗食管癌的初步指导。

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