首页> 美国卫生研究院文献>Iranian Journal of Pharmaceutical Research : IJPR >Combination of Ethanolic Extract of Citrus aurantifolia Peels with Doxorubicin Modulate Cell Cycle and Increase Apoptosis Induction on MCF-7 Cells
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Combination of Ethanolic Extract of Citrus aurantifolia Peels with Doxorubicin Modulate Cell Cycle and Increase Apoptosis Induction on MCF-7 Cells

机译:桔皮乙醇提取物与阿霉素的结合调节细胞周期并增加对MCF-7细胞的凋亡诱导

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摘要

New approach of breast cancer therapy is developed toward combination therapy with agents that have a specific molecular target. Our previous study showed that Citrus aurantifolia lime peels ethanolic extract (CPE) increased the sensitivity of MCF-7 cells againts doxorubicin. This study aims to observe the mechanism of combination CPE and doxorubicin in cell cycle modulation and apoptosis on MCF-7 cells. The assays were performed in the study were cell cycle assay, apoptosis induction, and immunocytochemistry of MCF-7 cells.The effect on the modulation of cell cycle and apoptosis were observed by flowcytometry assay in both single dose of CPE and its combination with Doxorubicin. Cell cycle distribution were observed with flowcytometer FACS-Calibur and its data was analyzed by Cell Quest program. Apoptotic induction in MCF-7 cells was examined using acrydine orange-ethidium bromide (AO-EtBr) double staining. Immunocytochemistry assay was done to observe the expression of apoptotic regulation protein p53 and Bcl-2. The result showed that CPE 6 μg/mL induced apoptosis and cell accumulation at G1 phase, while CPE 15 μg/mL induced apoptosis and cell accumulation at G2/M phase. The combination of doxorubicin 200 nM with CPE 6 μg/mL increased apoptosis induction than their single treatment, and cell accumulation at G2/M phase. Evidence of apoptosis and protein expression of p53 and Bcl-2 indicated that both single applications and combinations of CPE and doxorubicin are able to increase apoptotic bodies of MCF-7 cells by increasing the proteins expression. This result suggested that CPE could perform as co-chemotherapeutic agent with doxorubicin on breast cancer cells.
机译:乳腺癌治疗的新方法正在发展为与具有特定分子靶标的药物联合治疗。我们之前的研究表明,柑桔青柠皮果皮乙醇提取物(CPE)可提高MCF-7细胞对阿霉素的敏感性。本研究旨在观察CPE和阿霉素联合在MCF-7细胞的细胞周期调控和凋亡中的作用机制。本研究在细胞周期测定,凋亡诱导和MCF-7细胞免疫细胞化学方面进行了研究。流式细胞术检测了单剂量CPE及其与阿霉素的组合对细胞周期和凋亡的影响。用流式细胞仪FACS-Calibur观察细胞周期分布,并通过Cell Quest程序分析其数据。 MCF-7细胞凋亡诱导使用了丙烯酰橙-溴乙锭(AO-EtBr)双重染色。进行免疫细胞化学分析以观察凋亡调节蛋白p53和Bcl-2的表达。结果表明CPE 6μg/ mL诱导G1期细胞凋亡和细胞蓄积,而CPE 15μg/ mL诱导G2 / M期细胞凋亡和细胞蓄积。阿霉素200 nM与CPE 6μg/ mL的组合比单次治疗增加了细胞凋亡诱导,并增加了G2 / M期的细胞蓄积。 p53和Bcl-2凋亡和蛋白表达的证据表明,单次应用以及CPE和阿霉素的组合均可通过增加蛋白表达来增加MCF-7细胞的凋亡小体。该结果表明,CPE可以与阿霉素在乳腺癌细胞上作为联合化疗剂。

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