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黄腐酚,一种来自啤酒花的异戊烯基化查耳酮,可抑制多柔比星耐药MCF-7/ADR细胞的活力和干性。

Xanthohumol, a Prenylated Chalcone from Hops, Inhibits the Viability and Stemness of Doxorubicin-Resistant MCF-7/ADR Cells.

作者信息

Liu Ming, Yin Hua, Qian Xiaokun, Dong Jianjun, Qian Zhonghua, Miao Jinlai

机构信息

Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

State Key Laboratory of Biological Fermentation Engineering of Beer (In Preparation), Qingdao 266061, China.

出版信息

Molecules. 2016 Dec 28;22(1):36. doi: 10.3390/molecules22010036.

Abstract

Xanthohumol is a unique prenylated flavonoid in hops ( L.) and beer. Xanthohumol has been shown to possess a variety of pharmacological activities. There is little research on its effect on doxorubicin-resistant breast cancer cells (MCF-7/ADR) and the cancer stem-like cells exiting in this cell line. In the present study, we investigate the effect of xanthohumol on the viability and stemness of MCF-7/ADR cells. Xanthohumol inhibits viability, induces apoptosis, and arrests the cell cycle of MCF-7/ADR cells in a dose-dependent manner; in addition, xanthohumol sensitizes the inhibition effect of doxorubicin on MCF-7/ADR cells. Interestingly, we also find that xanthohumol can reduce the stemness of MCF-7/ADR cells evidenced by the xanthohumol-induced decrease in the colony formation, the migration, the percentage of side population cells, the sphere formation, and the down-regulation of stemness-related biomarkers. These results demonstrate that xanthohumol is a promising compound targeting the doxorubicin resistant breast cancer cells and regulating their stemness, which, therefore, will be applied as a potential candidate for the development of a doxorubicin-resistant breast cancer agent and combination therapy of breast cancer.

摘要

黄腐酚是啤酒花和啤酒中一种独特的异戊烯基黄酮。黄腐酚已被证明具有多种药理活性。关于其对多柔比星耐药乳腺癌细胞(MCF-7/ADR)及其细胞系中存在的癌症干细胞样细胞的影响,研究较少。在本研究中,我们研究了黄腐酚对MCF-7/ADR细胞活力和干性的影响。黄腐酚以剂量依赖性方式抑制MCF-7/ADR细胞的活力、诱导凋亡并使细胞周期停滞;此外,黄腐酚可增强多柔比星对MCF-7/ADR细胞的抑制作用。有趣的是,我们还发现黄腐酚可降低MCF-7/ADR细胞的干性,这可通过黄腐酚诱导的集落形成、迁移、侧群细胞百分比、球体形成减少以及干性相关生物标志物的下调来证明。这些结果表明,黄腐酚是一种有前景的化合物,可靶向多柔比星耐药乳腺癌细胞并调节其干性,因此将作为开发多柔比星耐药乳腺癌药物和乳腺癌联合治疗的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6875/6155764/3b4453e67b5f/molecules-22-00036-g001.jpg

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