Differential alteration of drug-metabolizing enzyme activities after cyclophosphamide/adriamycin administration in breast cancer patients
| dc.contributor.author | Elkiran, Tamer | |
| dc.contributor.author | Harputluoglu, H. | |
| dc.contributor.author | Yasar, U. | |
| dc.contributor.author | Babaoglu, M.O. | |
| dc.contributor.author | Dincel, A.K. | |
| dc.contributor.author | Altundag, K. | |
| dc.contributor.author | Bozkurf, A. | |
| dc.date.accessioned | 2026-08-12T16:10:43Z | |
| dc.date.issued | 2007 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | 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 study was designed to analyze the effects of CPA/ADR on these drug-metabolizing enzymes by using losartan 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/m2/day, 60 mg ADR/m2/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 interactions. © 2007 Prous Science. All rights reserved. | |
| dc.identifier.doi | 10.1358/mf.2007.29.1.1074690 | |
| dc.identifier.endpage | 32 | |
| dc.identifier.issn | 0379-0355 | |
| dc.identifier.issue | 1 | |
| dc.identifier.pmid | 17344941 | |
| dc.identifier.scopus | 2-s2.0-33947369020 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 27 | |
| dc.identifier.uri | https://doi.org/10.1358/mf.2007.29.1.1074690 | |
| dc.identifier.uri | https://hdl.handle.net/11508/42091 | |
| dc.identifier.volume | 29 | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.relation.ispartof | Methods and Findings in Experimental and Clinical Pharmacology | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_Scopus_20260511 | |
| dc.subject | Adriamycin; Cyclophosphamide; Cytochrome P450; Induction; Inhibition | |
| dc.title | Differential alteration of drug-metabolizing enzyme activities after cyclophosphamide/adriamycin administration in breast cancer patients | |
| dc.type | Article |







