共 22 条
Calycosin and Genistein Induce Apoptosis by Inactivation of HOTAIR/p-Akt Signaling Pathway in Human Breast Cancer MCF-7 Cells
被引:129
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Lin, Changrong
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Jiangbin Hosp Guangxi Zhuang Autonomous Reg, Dept Gen Surg, Nanning, Peoples R China Guilin Med Univ, Sch Basic Med Sci, Guilin 541004, Peoples R China

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[1] Guilin Med Univ, Sch Basic Med Sci, Guilin 541004, Peoples R China
[2] Jiangbin Hosp Guangxi Zhuang Autonomous Reg, Dept Gen Surg, Nanning, Peoples R China
[3] Guangxi Med Univ, Affiliated Hosp 1, Dept Emergency, Nanning, Peoples R China
[4] Guilin Med Univ, Dept Pathol, Guilin 541004, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Calycosin;
Genistein apoptosis;
HOTAIR;
p-Akt;
LONG NONCODING RNA;
PROLIFERATION;
EXPRESSION;
TARGETS;
D O I:
10.1159/000369732
中图分类号:
Q2 [细胞生物学];
学科分类号:
071013 [干细胞生物学];
摘要:
Background: Calycosin and genistein are the two main components of isoflavones. Previously, we reported that these compounds display antitumor activities in the breast cancer cell lines MCF-7 and T47D. In the present study, we investigated the mechanism of action of calycosin and genistein, and their respective efficacies as potential therapies for the treatment of breast carcinoma in the clinic. Methods: MCF-7 cells were treated with calycosin or genistein. Cell proliferation and apoptosis were measured using CCK8 assay and Hoechst 33258. The expression level of phosphorylated Akt protein was determined by western blotting. Expression level of HOTAIR was quantified by real-time PCR. Results: Both calycosin and genistein inhibited proliferation and induced apoptosis in MCF-7 breast cancer cells, especially after treatment with calycosin. Treatment of MCF-7 cells with calycosin or genistein resulted in decreased phosphorylation of Akt, and decreased expression of its downstream target, HOTAIR. Conclusion: Calycosin is more effective in inhibiting breast cancer growth in comparison with genistein, through its regulation of Akt signaling pathways and HOTAIR expression. Copyright (C) 2015 S. Karger AG, Basel
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页码:722 / 728
页数:7
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