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An evaluation of gemcitabines differential radiosensitising effect in related bladder cancer cell lines

机译:吉西他滨对相关膀胱癌细胞系的放射增敏作用的评估

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The aim of this study was to establish the radiosensitising properties of gemcitabine in a pair of related bladder tumour cell lines with differential radiosensitivity. The radioresistant bladder tumour cell line MGH-U1 and its radiosensitive mutant clone, S40b (both p53 mutant), had SF2 values (surviving fraction at 2?Gy) of 0.98 and 0.64, respectively (PμM gemcitabine radiosensitisation occurred only in the S40b cell line (dose-modifying factor (DMF)=1.4). At 0.3?μM (killing 50% of cells), both cell lines were radiosensitised; DMF=2.25 and 1.2 for MGH-U1 and S40b, respectively. These data suggest that gemcitabine is an effective radiosensitiser in bladder cancer cell lines, with greater sensitisation in the radioresistant parental line–a feature that should be useful in a clinical setting.
机译:这项研究的目的是建立吉西他滨在一对相关的具有不同放射敏感性的膀胱肿瘤细胞系中的放射敏感性。放射抗性膀胱肿瘤细胞系MGH-U1及其放射敏感性突变体克隆S40b(均为p53突变体)的SF2值(2?Gy的存活分数)分别为0.98和0.64(PμM吉西他滨放射致敏作用仅发生在S40b细胞系中) (剂量修饰因子(DMF)= 1.4),在0.3?μM(杀死​​50%的细胞)时,两个细胞系均被放射致敏; MGH-U1和S40b的DMF分别为2.25和1.2,这些数据表明吉西他滨在膀胱癌细胞系中是一种有效的放射增敏剂,在耐辐射的亲本系中具有更高的敏化度,这一特征在临床环境中应该有用。

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