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In vitro radiosensitisation by trabectedin in human cancer cell lines.

机译:trabectedin在人癌细胞系中的体外放射增敏作用。

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PURPOSE: To examine the potential radiosensitising properties of trabectedin (ET-743, Yondelis). METHODS AND MATERIALS: In vitro chemosensitivity was assessed in four tumour cell lines (DU145, HeLa, HT29, HOP62) by the crystal violet method. IC10s and IC50s were established for 1-h, 24-h and 7-day (continuous) exposure times. Radiosensitisation was evaluated by conventional colony assay. BrdUrd DNA-labelling and flow cytometry were used to analyse cell cycle kinetics. The rate of apoptotic induction was assed by annexyn-V labelling. RESULTS: Mean IC50s were 18.8 nM (10.5 - 30), 2.5 nM (1.5 - 5) and 0.25 nM (0.2-0.8) for 1 h, 24 h and continuous exposure times, respectively. HT29 and HOP62 were the most sensitive cells lines to trabectedin. Radiosensitisation was observed in DU145 and HeLa cells with a dose enhancement factor (DEF) of 1.92 and 1.77 at IC50 dose level, respectively. Trabectedin induced early S phase arrest in all cell lines studied. CONCLUSIONS: Trabectedin, at pharmacologically appropriated concentrations, harbours a significant in vitro radiosensitising effect and induces cell cycle changes and apoptosis in several human cancer cell lines. Further studies to define the clinical potential of the combination of trabectedin and radiotherapy are needed.
机译:目的:检查trabectedin(ET-743,Yandelis)的潜在放射增敏特性。方法和材料:采用结晶紫法评估了四种肿瘤细胞系(DU145,HeLa,HT29,HOP62)的体外化学敏感性。确定IC10和IC50的暴露时间为1小时,24小时和7天(连续)。通过常规菌落分析评估放射增敏作用。 BrdUrd DNA标记和流式细胞仪用于分析细胞周期动力学。通过膜联蛋白-V标记评估凋亡诱导率。结果:1小时,24小时和连续暴露时间的平均IC50分别为18.8 nM(10.5-30),2.5 nM(1.5-5)和0.25 nM(0.2-0.8)。 HT29和HOP62对trabectedin最敏感。在DU145和HeLa细胞中观察到放射增敏,在IC50剂量水平下的剂量增强因子(DEF)分别为1.92和1.77。 Trabectedin诱导了所有研究细胞系的早期S期阻滞。结论:特拉比丁在药理学上适当的浓度下具有显着的体外放射增敏作用,并诱导了几种人类癌细胞系的细胞周期变化和凋亡。需要进一步的研究来确定曲贝汀与放疗结合的临床潜力。

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