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P-aminosalicylate metabolism in cancer patients sensitive and resistant to chemotherapy

机译:对化疗敏感和耐药的癌症患者的对氨基水杨酸代谢

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摘要

A reduced response of a tumour to chemotherapy may be due to the host's drug metabolism. To test this hypothesis, we measured the metabolism of a model drug, para-aminosalicylate (PAS). Volunteers and cancer patients ingested a single oral dose (2 g) of PAS and we measured the plasma disappearance curve of the drug and its metabolite. In 7 patients suffering from lymphosarcoma, acute or chronic leukaemia and resistant to cancer chemotherapy, we observed low plasma PAS concentrations, an increase in PAS acetylation and an increased number (and a higher frequency) of abnormal liver-function tests. In 14 patients with malignant blood disease, yet responding well to chemotherapy, the metabolism of PAS is similar to that of healthy controls of the same age and sex. The plasma half-life of PAS is similar in sensitive and resistant patients, but slightly longer than in volunteers. Finally, in urine collected 120 min after drug administration, we observed the same results as in plasma. In conclusion, cancer patients resistant to chemotherapy do not metabolize the model drug PAS as volunteers or sensitive patients do, and this might be relevant to the terminal stage of the disease.
机译:肿瘤对化学疗法的反应降低可能是由于宿主的药物代谢所致。为了验证这一假设,我们测量了模型药物对氨基水杨酸酯(PAS)的代谢。志愿者和癌症患者摄入单次口服剂量(2克)的PAS,我们测量了该药物及其代谢产物的血浆消失曲线。在7名患有淋巴肉瘤,急性或慢性白血病并且对癌症化学疗法有抗药性的患者中,我们观察到血浆PAS浓度低,PAS乙酰化程度增加以及异常肝功能检查的次数(以及频率更高)增加。在14例恶性血液病患者中,对化疗反应良好,PAS的代谢与相同年龄和性别的健康对照者相似。在敏感和耐药的患者中,PAS的血浆半衰期相似,但比志愿者更长。最后,在给药后120分钟收集的尿液中,我们观察到与血浆中相同的结果。总之,对化疗耐药的癌症患者不会像志愿者或敏感患者那样代谢模型药物PAS,这可能与疾病的晚期有关。

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