TAO Yi-ming, HONG Xue, MA Yi-li, et al. Effects of Aloe Emodin Alone and in Combination with Cisplatin on Cell Proliferation and Apoptosis of Breast Cancer Cell Line MDA-MB-231[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(20): 127-130.
DOI:
TAO Yi-ming, HONG Xue, MA Yi-li, et al. Effects of Aloe Emodin Alone and in Combination with Cisplatin on Cell Proliferation and Apoptosis of Breast Cancer Cell Line MDA-MB-231[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(20): 127-130. DOI: 10.13422/j.cnki.syfjx.2015200127.
Effects of Aloe Emodin Alone and in Combination with Cisplatin on Cell Proliferation and Apoptosis of Breast Cancer Cell Line MDA-MB-231
MTT法检测细胞增殖;Annexin V FITC/PI双染和流式细胞术检测细胞凋亡与细胞周期;Western blot分析Bcl-2相关X蛋白(Bax)
B细胞淋巴瘤/白血病-2(Bcl-2)和Bcl-xL蛋白表达的变化。结果:与空白组比较
AE单用显著抑制乳腺癌细胞MDA-MB-231的增殖
半数抑制浓度(IC50)为22.21 μmol·L-1
与CP联用时IC50为9.51 μmol·L-1。联用指数CI50<1
表明两药物有协同作用;AE单用使细胞周期阻滞在G1期
并诱导细胞凋亡
联用CP则增强阻滞
凋亡率明显增加;两药联用显著抑制Bcl-2和Bcl-xL的表达
并上调Bax的表达
与空白组比较均具有明显的统计学差异(P<0.05
P<0.01)。结论:芦荟大黄素抑制乳腺癌MDA-MB-231细胞增殖
使细胞周期阻滞在G1期
并通过上调促凋亡蛋白和下调抗凋亡蛋白
诱导凋亡。与顺铂联用能增强其促凋亡作用
两药存在协同作用。
Abstract
Objective: To investigate the anti-proliferation and apoptosis effects of aloe emodin (AE) alone and in combination with cisplatin (AE-CP) on breast cancer cell MDA-MB-231. Method: MDA-MB-231 cells were treated for 48 h with 5
10
20
30
40
50 μmol·L-1 AE
2
4
8
12
24
36 μmol·L-1 CP or various concentrations of AE-CP. Cell proliferation was detected by MTT. Apoptosis and cell cycle were detected by Annexin V FITC/PI double-staining and flow cytometer. The protein levels of Bax
Bcl-2 and Bcl-xL were analyzed by Western blot. Result: AE alone significantly inhibited cell proliferation
with an IC50 of 22.21 μmol·L-1. IC50 decreased to 9.51 μmol·L-1 when it was used in combination with CP. The combination index CI50<1
indicating a synergic effect. AE alone arrested cell cycle in G1 phase and induced apoptosis. The arrest was accentuated when CP was given simultaneously
accompanied by a marked increment of apoptosis rate. AE-CP significantly inhibited the protein levels of Bcl-2 and Bcl-xL
but increased Bax. Conclusion: AE could inhibit the cell proliferation of MDA-MB-231
arrest the cell cycle in G1 phase
and induce apoptosis by increasing apoptosis proteins and decreasing anti-apoptosis proteins. AE shows a synergic effect of apoptosis when combined with CP.
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Effect of Shenqi Fuzheng Injection in Improving Sensitivity of Human Breast Cancer MDA-MB-231 Cells to Cisplatin Through Tumor Associated Macrophages
Effect of Astragalus Polysaccharide on Growth and Tumor-related Apoptosis Protein of Human Breast Cancer MDA-MB-231 Transplanted Tumor in Nude Mice
Effects of Breviscapine on Renal Cell Apoptosis and Expression of Apoptosis-related Proteins in Mice with Cisplatin-induced Nephrotoxicity
Effects of Extract on Proliferation, Apoptosis and Caspase-3 Expression in Human Breast Cancer MCF-7 Cells
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