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Enhancement of the anti-tumour effect of cyclophosphamide by the bioreductive drugs AQ4N and tirapazamine

机译:生物还原药物AQ4N和替拉帕明增强环磷酰胺的抗肿瘤作用

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摘要

The ability of the bioreductive drugs AQ4N and tirapazamine to enhance the anti-tumour effect of cyclophosphamide was assessed in three murine tumour models. In male BDF mice implanted with the T50/80 mammary carcinoma, AQ4N (50–150 mg kg−1) in combination with cyclophosphamide (100 mg kg−1) produced an effect equivalent to a single 200 mg kg−1dose of cyclophosphamide. Tirapazamine (25 mg kg−1) in combination with cyclophosphamide (100 mg kg−1) produced an effect equivalent to a single 150 mg kg−1dose of cyclophosphamide. In C3H mice implanted with the SCCVII or RIF-1 tumours, enhancement of tumour cell killing was found with both drugs in combination with cyclophosphamide (50–200 mg kg−1); AQ4N (50–200 mg kg−1) produced a more effective combination than tirapazamine (12.5–50 mg kg−1). Unlike tirapazamine, which showed a significant increase in toxicity to bone marrow cells, the combination of AQ4N (100 mg kg−1) 6 h prior to cyclophosphamide (100 mg kg−1) resulted in no additional toxicity towards bone marrow cells compared to that caused by cyclophosphamide alone. In conclusion, AQ4N gave a superior anti-tumour effect compared to tirapazamine when administered with a single dose of cyclophosphamide (100 mg kg−1). © 2000 Cancer Research Campaign
机译:在三种鼠类肿瘤模型中评估了生物还原药AQ4N和替拉帕明增强环磷酰胺抗肿瘤作用的能力。在植入了T50 / 80乳腺癌的雄性BDF小鼠中,AQ4N(50–150 mg kg-1)与环磷酰胺(100 mg kg-1)联合产生的效果相当于一次200 mg kg-1剂量的环磷酰胺。替拉帕明(25 mg kg-1)与环磷酰胺(100 mg kg-1)的结合产生的效果等同于单剂量150 mg kg-1剂量的环磷酰胺。在植入了SCCVII或RIF-1肿瘤的C3H小鼠中,两种药物与环磷酰胺(50-200 mg kg-1)联合使用均能增强肿瘤细胞的杀伤力。 AQ4N(50–200 mg kg-1)产生的组合比替拉帕明(12.5–50 mg kg-1)更有效。与替拉帕明不同,后者对骨髓细胞的毒性显着增加,与环磷酰胺(100 mg kg-1)相比,AQ4N(100 mg kg-1)联合使用6 h之前对骨髓细胞没有额外的毒性仅由环磷酰胺引起。总之,当与单剂量环磷酰胺(100 mg kg-1)一起给药时,与替拉帕明相比,AQ4N具有更好的抗肿瘤作用。 ©2000癌症研究运动

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