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粉防己碱抑制人乳腺癌MDA-MB-231细胞的迁移并导致其凋亡。

Fangchinoline inhibits migration and causes apoptosis of human breast cancer MDA-MB-231 cells.

作者信息

Wang Binggao, Xing Zhibo, Wang Fengmei, Yuan Xinyan, Zhang Yanhui

机构信息

Breast Center, Qingdao Central Hospital, Qingdao, Shandong 266033, P.R. China.

Department of Cardiology, Qingdao Central Hospital, Qingdao, Shandong 266033, P.R. China.

出版信息

Oncol Lett. 2017 Nov;14(5):5307-5312. doi: 10.3892/ol.2017.6831. Epub 2017 Aug 25.

Abstract

In order to improve outcomes after breast cancer treatment, it is essential to understand the mechanisms of action of potential therapeutic agents. The effect of fangchinoline (FAN) on migration and apoptosis of human breast cancer MDA-MB-231 cells and its underlying mechanisms were investigated. MDA-MB-231 cells were treated with different concentrations of FAN, growth inhibition rates were measured by MTT assay and morphological changes of apoptotic cells were observed by Hoechst staining. The wound-healing assay was used to determine of the effect of FAN on the migration of MDA-MB-231 cells. ELISA was used to detect the expression of MMP-2 and -9 in MDA-MB-231 cells treated with different concentrations of FAN and western blot analysis was used to quantify expression of NF-κβ and Iκβ proteins in the same cells. Our results showed that FAN significantly inhibited the growth of MDA-MB-231 cells in concentration-dependent manner and it induced MDA-MB-231 cell apoptosis. With the high FAN concentrations and long exposure times, the levels of MMP-2 and -9 decreased and the expression of NF-κβ decreased, while the expression of Iκβ protein increased. Based on these results, the antitumor effects of FAN on breast cancer cells can be explained at least partially by inducing apoptosis and inhibiting the migration of MDA-MB-231 cells.

摘要

为了改善乳腺癌治疗后的效果,了解潜在治疗药物的作用机制至关重要。研究了粉防己碱(FAN)对人乳腺癌MDA-MB-231细胞迁移和凋亡的影响及其潜在机制。用不同浓度的FAN处理MDA-MB-231细胞,通过MTT法测定生长抑制率,并用Hoechst染色观察凋亡细胞的形态变化。采用伤口愈合试验来确定FAN对MDA-MB-231细胞迁移的影响。用ELISA检测不同浓度FAN处理的MDA-MB-231细胞中MMP-2和-9的表达,并用蛋白质印迹分析法定量同一细胞中NF-κβ和Iκβ蛋白的表达。我们的结果表明,FAN以浓度依赖性方式显著抑制MDA-MB-231细胞的生长,并诱导MDA-MB-231细胞凋亡。随着FAN浓度的升高和作用时间的延长,MMP-2和-9的水平降低,NF-κβ的表达降低,而Iκβ蛋白的表达增加。基于这些结果,FAN对乳腺癌细胞的抗肿瘤作用至少部分可以通过诱导凋亡和抑制MDA-MB-231细胞的迁移来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b75a/5652195/86ed09549010/ol-14-05-5307-g00.jpg

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