首页> 外文期刊>Acta Poloniae Pharmaceutica: Durg Research >Effect of adriblastin on viability, cell cycle and apoptosis in B16 and cloudman s91 mouse melanoma cells in vitro.
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Effect of adriblastin on viability, cell cycle and apoptosis in B16 and cloudman s91 mouse melanoma cells in vitro.

机译:阿德霉素对B16和cloudman s91小鼠黑素瘤细胞体外活力,细胞周期和凋亡的影响。

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Recently, the oncologists have been increasingly interested in apoptosis. which is morphologically. biochemically and topographically different from necrosis. Apoptosis is probably a key point to understand the resistance of malignant cells to cytotoxic drug. The aim of this study was to determine the influence of adriblastin on morphology and kinetics of cell proliferation and evaluation of apoptosis and necrosis in B16 and Cl S91 mouse melanoma cells in vitro. Adriblastin induced morphological changes indicating occurrence of apoptosis and necrosis in B16 and Cl S91 mouse melanoma cells. The number of viable B16 and Cl S91 cells was estimated by flow cytometry analysis. Apoptotic cells were detected using the annexin V-FITC test. DNA content, after staining cells with propidium iodide, was analysed by flow cytometry. B16 cell line was more sensitive to adriblastin treatment than the CIS91 cell line. The adriblastin EC50, value estimated for the B16 line was 2.4 microM. while for Cl S91 line was 4.0 microM. It was revealed that about 59% Cl S91 cells and 65% B16 cells had died in the apoptotic way after adriblastin addition at EC50, concentration to B16 and Cl S91 cultures. Adriblastin induced cell arrest in G1 and S cell cycle phase in both B16 and Cl S91 cell lines. CONCLUSION: the new solutions to determinate cell chemosensitivity should be introduced into clinical practice.
机译:最近,肿瘤学家对细胞凋亡越来越感兴趣。从形态上讲在生化和地形上不同于坏死。凋亡可能是了解恶性细胞对细胞毒性药物耐药性的关键点。这项研究的目的是确定在体外,Adriblastin对B16和Cl S91小鼠黑素瘤细胞的形态和动力学的影响以及细胞凋亡和坏死的评估。 Adriblastin诱导的形态变化表明B16和Cl S91小鼠黑素瘤细胞发生凋亡和坏死。通过流式细胞术分析估计存活的B16和C1 S91细胞的数目。使用膜联蛋白V-FITC测试检测凋亡细胞。用碘化丙啶染色细胞后,通过流式细胞仪分析DNA含量。与CIS91细胞系相比,B16细胞系对成纤维细胞的处理更为敏感。对于B16品系,估计的adriblastin EC50值为2.4 microM。 Cl S91系为4.0 microM。结果表明,在EC50浓度,B16和Cl S91培养液浓度下,添加成纤维蛋白后,约有59%的Cl S91细胞和65%的B16细胞以凋亡的方式死亡。 Adriblastin诱导B16和Cl S91细胞系的G1和S细胞周期阶段的细胞停滞。结论:确定细胞化学敏感性的新方法应引入临床实践。

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