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首页> 外文期刊>Cancer Cell International >Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line
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Modulation of doxorubicin cytotoxicity by resveratrol in a human breast cancer cell line

机译:白藜芦醇对人乳腺癌细胞系中阿霉素细胞毒性的调节

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Background Breast cancer is the most common cancer in the Arab world and it ranked first among Saudi females. Doxorubicin (DOX), an anthracycline antibiotic is one of the most effective anticancer agents used to treat breast cancer. chronic cardiotoxicity is a major limiting factor of the use of doxorubicin. Therefore, our study was designed to assess the role of a natural product resveratrol (RSVL) on sensitization of human breast cancer cells (MCF-7) to the action of DOX in an attempt to minimize doxorubicin effective dose and thereby its side effects. Methods Human breast cancer cell line MCF-7, was used in this study. Cytotoxic activity of DOX was determined using (sulforhodamine) SRB method. Apoptotic cells were quantified after treatment by annexin V-FITC- propidium iodide (PI) double staining using flow-cytometer. Cell cycle disturbance and doxorubicin uptake were determined after RSVL or DOX treatment. Results Treatment of MCF-7 cells with 15 μg/ml RSVL either simultaneously or 24 h before DOX increased the cytotoxicity of DOX, with IC50 were 0.056 and 0.035 μg/ml, respectively compared to DOX alone IC50 (0.417 μg/ml). Moreover, flow cytometric analysis of the MCF-7 cells treated simultaneously with DOX (0.5 μg/ml) and RSVL showed enhanced arrest of the cells in G0 (80%). On the other hand, when RSVL is given 24 h before DOX although there was more increased in the cytotoxic effect of DOX against the growth of the cells, however, there was decreased in percentage arrest of cells in G0, less inhibition of DOX-induced apoptosis and reduced DOX cellular uptake into the cells. Conclusion RSVL treatment increased the cytotoxic activity of DOX against the growth of human breast cancer cells when given either simultaneously or 24 h before DOX.
机译:背景技术乳腺癌是阿拉伯世界中最常见的癌症,在沙特女性中排名第一。阿霉素(Doxorubicin,DOX)是一种蒽环类抗生素,是用于治疗乳腺癌的最有效的抗癌药之一。慢性心脏毒性是使用阿霉素的主要限制因素。因此,我们的研究旨在评估天然产物白藜芦醇(RSVL)对人乳腺癌细胞(MCF-7)对DOX作用的敏化作用,以试图将阿霉素有效剂量减至最小。方法采用人乳腺癌细胞MCF-7。 DOX的细胞毒活性是使用(磺胺多巴胺)SRB法测定的。使用流式细胞仪通过膜联蛋白V-FITC-碘化丙啶(PI)双重染色处理后,对凋亡细胞进行定量。在RSVL或DOX处理后测定细胞周期紊乱和阿霉素摄取。结果与DOX单独使用IC50(0.417μg/ ml)相比,DOX同时或在DOX之前24 h用15μg/ ml RSVL处理MCF-7细胞会增加DOX的细胞毒性,IC50分别为0.056和0.035μg/ ml。此外,用DOX(0.5μg/ ml)和RSVL同时处理的MCF-7细胞的流式细胞仪分析显示,细胞在G 0 中的阻滞作用增强(80%)。另一方面,当在DOX前24小时给予RSVL时,尽管DOX对细胞生长的细胞毒性作用增加更多,但是,G 0 ,对DOX诱导的细胞凋亡的抑制作用降低,并且减少了DOX细胞对细胞的摄取。结论RSVL治疗在DOX同时或24 h给药时可增加DOX对人乳腺癌细胞生长的细胞毒活性。

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