Differential alteration of drug-metabolizing enzyme activities after cyclophosphamide/adriamycin administration in breast cancer patients

被引:13
作者
Elkiran, T. [1 ]
Harputhioglu, H.
Yasar, U.
Babaoglu, M. O.
Dincel, A. K.
Altundag, K.
Ozisik, Y.
Guler, N.
Bozkurt, A.
机构
[1] Hacettepe Univ, Inst Oncol, Dept Med Oncol, Ankara, Turkey
[2] Hacettepe Univ, Fac Med, Dept Pharmacol, TR-06100 Ankara, Turkey
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 2007年 / 29卷 / 01期
关键词
adriamycin; cyclophosphamide; cytochrome P450; induction; inhibition;
D O I
10.1358/mf.2007.29.1.1074690
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cyclophosphamide (CPA) and adriamycin (ADR) are widely used drugs for cancer chemotherapy. It has been reported that CPA and ADR singly or in combination could alter activities of a variety of drug-metabolizing enzymes in animals via multiple mechanisms. However, the effects of CPA/ADR on drug metabolism are largely unknown in human beings. Losartan metabolism has been suggested as a marker for determination of CYP2C9 activity. Caffeine is a commonly used probe to assess the metabolic activities of CYP1A2. CYP2A6. N-acetyltransferase 2 (NAT2) and xanthine oxidase (XO). The present present study was designed to analyze the effects of CPA/ADR on these drugs-metabolizing enzymes by using lasartan and caffeine as probe drugs. A single oral dose of 25 mg losartan and a cup of instant coffee was given to 15 breast cancer patients on three occasions (before, and 2-4 h and 3 weeks after the adjuvant CPA/ADR chemotherapy [600 mg CPA/m(2)/day.60 mg ADR/m(2)/day]). Losartan, caffeine and their metabolites were analyzed by using high-pressure liquid chromatography. When compared with baseline. CYP1A2 activity was increased by 20% and CYP2C9 activity was decreased by 315% 3 weeks after the administration of CPA/ADR chemotherapy (p = 0.05). The chemotherapy did not change the activities of CYP2A6, NAT2 or XO. CPA/ADR treatment caused a differential effect on drug-metabolizing enzyme activities and this may contribute to predicting the efficacy and toxicity of chemotherapeutics, as well as understanding the drug-drug interaction. (c) 2007 Prous Science. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
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