Monochasma Savatieri 水提取物可抑制人类乳腺癌细胞株的迁移和粘附,且不会产生毒性

IF 2.6 4区 医学 Q3 CHEMISTRY, MEDICINAL Anti-cancer agents in medicinal chemistry Pub Date : 2024-04-17 DOI:10.2174/0118715206287870240408031843
Lin Tan, Juan C. Solis-Sainz
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Immunofluorescent assays confirmed caveolin-1 expression in MDA-MB-231 cells. method: Cell viability, migration, adhesion, circularity, and cell cycle were evaluated by crystal violet staining, wound-healing and transwell assays and flow cytometry in MCF7 and MDA-MB-231 cells. Caveolin-1, snail, vimentin and activated Erk and Akt expression were determined by western blot in MDA-MB-231 cells. Caveolin-1 expression in MDA-MB-231 cells was confirmed by immunofluorescent assays. Results: Survival and cell cycle of MCF7 and MDA-MB-231 cells were not modified by doses up to 500 μg/mL of the extract. The extract inhibited cell migration and adhesion of MDA-MB-231 cells. When cells were exposed to the extract, there was a slight decrease in protein expression of factors related to epithelial-to-mesenchymal transition (snail and vimentin) and a strong decrease in the expression of the oncogenic membrane protein caveolin- 1. Furthermore, the levels of phosphorylated Erk and Akt were also decreased. The content of acteoside, a phenylpropanoid glycoside with reported anti-cancer activity present in M. savatieri, was almost 5 times as much as isoacteoside. Conclusion: M. savatieri possesses anti-cancer activity without exerting cytotoxicity on breast cancer cells. The extract exhibited anti-migratory and anti-adhesion effects on breast cancer cells by regulating Erk and Akt signaling pathways and the expression of caveolin-1. In addition, acteoside present in M. savatieri could be responsible for the observed effects. conclusion: M. savatieri possesses anti-cancer activity without exerting cytotoxicity on breast cancer cells. The extract exerted anti-migratory and anti-adhesion effects on breast cancer cells by regulating Erk and Akt signaling pathways and the expression of caveolin-1. 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引用次数: 0

摘要

背景介绍野漆树(Monochasma savatieri)是一种罕见的濒危植物,在中国传统医学中被用来治疗癌症。研究目的通过测定蝙蝠蛾水提取物对乳腺癌细胞的细胞毒性、抗迁移和抗粘附作用,评估其抗癌活性:通过测定 M. savatieri 水提取物对乳腺癌细胞的细胞毒性、抗迁移和抗粘附作用,评估其抗癌活性。研究方法在 MCF7 和 MDA-MB-231 细胞中,通过水晶紫(CV)染色、伤口愈合、透孔试验和流式细胞术评估细胞活力、迁移、粘附、圆周率和细胞周期。MDA-MB-231细胞中的Caveolin-1、蜗牛、波形蛋白以及活化的Erk和Akt的表达是通过Western印迹法测定的。免疫荧光检测证实了洞穴素-1 在 MDA-MB-231 细胞中的表达:在 MCF7 和 MDA-MB-231 细胞中,通过水晶紫染色、伤口愈合和透孔试验以及流式细胞术评估细胞活力、迁移、粘附、圆周率和细胞周期。MDA-MB-231 细胞中的 Caveolin-1、蜗牛、波形蛋白以及活化的 Erk 和 Akt 的表达是通过 Western 印迹法测定的。免疫荧光试验证实了 Caveolin-1 在 MDA-MB-231 细胞中的表达。结果剂量高达 500 μg/mL 的提取物不会改变 MCF7 和 MDA-MB-231 细胞的存活率和细胞周期。提取物抑制了 MDA-MB-231 细胞的迁移和粘附。当细胞暴露于萃取物时,上皮细胞向间质转化相关因子(蜗牛和波形蛋白)的蛋白表达量略有下降,而致癌膜蛋白洞穴素-1的表达量则大幅下降。 此外,磷酸化的Erk和Akt的水平也有所下降。据报道,M. savatieri 中含有一种具有抗癌活性的苯基丙酮甙--肌苷,其含量几乎是异肌苷的 5 倍。结论M. savatieri 具有抗癌活性,但不会对乳腺癌细胞产生细胞毒性。该提取物通过调节 Erk 和 Akt 信号通路以及 caveolin-1 的表达,对乳腺癌细胞具有抗迁移和抗粘附作用。此外,M. savatieri 中的肌动球蛋白苷可能是产生这些效果的原因:M. savatieri具有抗癌活性,但不会对乳腺癌细胞产生细胞毒性。该提取物通过调节 Erk 和 Akt 信号通路以及洞穴素-1 的表达,对乳腺癌细胞产生抗迁移和抗粘附作用。此外,M. savatieri 中的肌动球蛋白苷可能是产生这些作用的原因。
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Monochasma Savatieri Aqueous Extract inhibits Human Breast Cancer Cell Line Migration and Adhesion Without Generating Toxicity
Background: Monochasma savatieri, is a rare and endangered plant used to treat cancer in Chinese traditional medicine. Objective: To evaluate the anti-cancer activity of M. savatieri aqueous extract by determining its cytotoxicity, anti-migratory, and anti-adhesion effects on breast cancer cells. objective: To evaluate the anti-cancer activity of M. savatieri aqueous extract by determining its cytotoxicity, anti-migratory and anti-adhesion effects on breast cancer cells. Methods: Cell viability, migration, adhesion, circularity, and cell cycle were evaluated by crystal violet (CV) staining, wound-healing, and transwell assays and flow cytometry in MCF7 and MDA-MB-231 cells. Caveolin-1, snail, vimentin and activated Erk and Akt expression were determined by western blot in MDA-MB-231 cells. Immunofluorescent assays confirmed caveolin-1 expression in MDA-MB-231 cells. method: Cell viability, migration, adhesion, circularity, and cell cycle were evaluated by crystal violet staining, wound-healing and transwell assays and flow cytometry in MCF7 and MDA-MB-231 cells. Caveolin-1, snail, vimentin and activated Erk and Akt expression were determined by western blot in MDA-MB-231 cells. Caveolin-1 expression in MDA-MB-231 cells was confirmed by immunofluorescent assays. Results: Survival and cell cycle of MCF7 and MDA-MB-231 cells were not modified by doses up to 500 μg/mL of the extract. The extract inhibited cell migration and adhesion of MDA-MB-231 cells. When cells were exposed to the extract, there was a slight decrease in protein expression of factors related to epithelial-to-mesenchymal transition (snail and vimentin) and a strong decrease in the expression of the oncogenic membrane protein caveolin- 1. Furthermore, the levels of phosphorylated Erk and Akt were also decreased. The content of acteoside, a phenylpropanoid glycoside with reported anti-cancer activity present in M. savatieri, was almost 5 times as much as isoacteoside. Conclusion: M. savatieri possesses anti-cancer activity without exerting cytotoxicity on breast cancer cells. The extract exhibited anti-migratory and anti-adhesion effects on breast cancer cells by regulating Erk and Akt signaling pathways and the expression of caveolin-1. In addition, acteoside present in M. savatieri could be responsible for the observed effects. conclusion: M. savatieri possesses anti-cancer activity without exerting cytotoxicity on breast cancer cells. The extract exerted anti-migratory and anti-adhesion effects on breast cancer cells by regulating Erk and Akt signaling pathways and the expression of caveolin-1. In addition, acteoside present in M. savatieri could be responsible for the observed effects.
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来源期刊
Anti-cancer agents in medicinal chemistry
Anti-cancer agents in medicinal chemistry ONCOLOGY-CHEMISTRY, MEDICINAL
CiteScore
5.10
自引率
3.60%
发文量
323
审稿时长
4-8 weeks
期刊介绍: Formerly: Current Medicinal Chemistry - Anti-Cancer Agents. Anti-Cancer Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of anti-cancer agents. Each issue contains a series of timely in-depth reviews and guest edited issues written by leaders in the field covering a range of current topics in cancer medicinal chemistry. The journal only considers high quality research papers for publication. Anti-Cancer Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in cancer drug discovery.
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