Comparative effect of sodium butyrate and sodium propionate on proliferation, cell cycle and apoptosis in human breast cancer cells MCF-7

MCF-7型 丁酸钠 细胞周期 碘化丙啶 丁酸盐 细胞生长 细胞凋亡 午睡 丙酸钠 癌症研究 化学 癌细胞 MTT法 内科学 分子生物学 生物化学 流式细胞术 丙酸盐 生物 癌症 医学 程序性细胞死亡 发酵 人体乳房 神经科学 基因
作者
Josiane Semaan,Sandy El-Hakim,José-Noël Ibrahim,Rémi Safi,Arpiné Ardzivian Elnar,Charbel El Boustany
出处
期刊:Breast Cancer [Springer Science+Business Media]
卷期号:27 (4): 696-705 被引量:58
标识
DOI:10.1007/s12282-020-01063-6
摘要

Short-chain fatty acids (SCFAs) are ubiquitous lipids produced as a result of bacterial fermentation of dietary fiber. While their role in colorectal cancer is well known, the effect of SCFAs in breast cancer is poorly defined. To understand the various effects of SCFAs on breast carcinogenesis, we investigated the effect of sodium butyrate (NaB) and sodium propionate (NaP) in MCF-7 cell line. Cells were incubated with different concentrations of NaB or NaP for 24, 48, 72 or 96 h. Cell proliferation was assayed using MTT kit. Cell cycle was performed using propidium iodide staining then analyzed with a flow cytometer. Apoptosis was assessed by Hoechst technique and cell-cycle sub-G1 phase. NaB and NaP inhibited MCF-7 cell proliferation in a dose-dependent manner with respective IC50 of 1.26 mM and 4.5 mM, thus indicating that NaB is more potent than NaP. Low and medium levels of both SCFAs induced morphology changes which are characteristic of a differentiated phenotype. Flow cytometry analysis revealed a blockage in G1 growth phase. Interestingly, removing NaB or NaP from culture media after few days of treatment showed a reversible effect on cell morphology and proliferation where cells reentered the cycle after 24 h of drug wash-out. Finally, treatment with medium levels of these molecules induced low MCF-7 apoptosis, while higher doses led to massive apoptosis. Our results show that SCFAs may be considered as an interesting inhibitor for breast cancer progression.
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