Tamoxifen inhibits cytochrome P4502C9 activity in breast cancer patients

被引:21
作者
Boruban, M. C.
Yasar, U. [1 ]
Babaoglu, M. O.
Sencan, O.
Bozkurt, A.
机构
[1] Univ Hacettepe, Fac Med, Dept Pharmacol, TR-06100 Ankara, Turkey
[2] SSK Hosp, Ankara, Turkey
关键词
tarnoxifen; CYP2C9; inhibition; drug-drug interaction;
D O I
10.1179/joc.2006.18.4.421
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Tamoxifen has been reported to potentiate the anticoagulant effect of warfarin and also to increase the plasma level of phenytoin, which are mainly metabolized by CYP2C9. The aim of this study was to determine the influence of tamoxifen on CYP2C9 activity in vivo in humans. Thirteen breast cancer patients who would start tamoxifen following cytotoxic chemotherapy were enrolled in the study. A single oral dose of 2 5 mg losartan was given to the patients 2 days before and 2 weeks after starting tamoxifen therapy. Losartan and E3174 in 8-hour urine samples were measured by HPLC. Tamoxifen significantly increased the average urinary losartan/E3174 ratio from 0.73 (CI95%=0.15-2.30) to 1.66 (Cl-95%=0.68-5.20), after 2 weeks of treatment (p=0.002). Tamoxifen inhibited CYP2C9 activity in breast cancer patients within two weeks of its administration. The inhibition of CYP2C9 activity may be a possible explanation for the drug-drug interaction of tamoxifen with CYP2C9 substrates.
引用
收藏
页码:421 / 424
页数:4
相关论文
共 21 条
[1]
Functional impact of CYP2C*5, CYP2C9*6, CYP2C9*8, and CYP2C9*11 in vivo among black Africans [J].
Allabi, AC ;
Gala, JL ;
Horsmans, Y ;
Babaoglu, MO ;
Bozkurt, A ;
Heusterspreute, M ;
Yasar, U .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2004, 76 (02) :113-118
[2]
CYP2C9 genetic variants and losartan oxidation in a Turkish population [J].
Babaoglu, MO ;
Yasar, U ;
Sandberg, M ;
Eliasson, E ;
Dahl, ML ;
Kayaalp, SO ;
Bozkurt, A .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 60 (05) :337-342
[3]
Identification of human CYP forms involved in the activation of tamoxifen and irreversible binding to DNA [J].
Boocock, DJ ;
Brown, K ;
Gibbs, AH ;
Sanchez, E ;
Turteltaub, KW ;
White, INH .
CARCINOGENESIS, 2002, 23 (11) :1897-1901
[4]
Oxidative metabolism of tamoxifen to Z-4-hydroxy-tamoxifen by cytochrome P450 isoforms:: An appraisal of in vitro studies [J].
Coller, JK .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (11) :845-848
[5]
CYP2D6 genotype, antidepressant use, and tamoxifen metabolism during adjuvant breast cancer treatment [J].
Jin, Y ;
Desta, Z ;
Stearns, V ;
Ward, B ;
Ho, H ;
Lee, KH ;
Skaar, T ;
Storniolo, AM ;
Li, L ;
Araba, A ;
Blanchard, R ;
Nguyen, A ;
Ullmer, L ;
Hayden, J ;
Lemler, S ;
Weinshilboum, RM ;
Rae, JM ;
Hayes, DF ;
Flockhart, DA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (01) :30-39
[6]
Clinical consequences of cytochrome P4502C9 polymorphisms [J].
Kirchheiner, J ;
Brockmöller, J .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 77 (01) :1-16
[7]
Dose-dependent inhibition of the CYP2D6 catalyzed oxidation of sparteine by mepyramine in healthy volunteers [J].
Kortunay, S ;
Bozkurt, A ;
Basci, NE ;
Brosen, K ;
Kayaalp, SO .
PHARMACOLOGY & TOXICOLOGY, 2001, 89 (06) :331-334
[8]
Effects of terfenadine and diphenhydramine on the CYP2D6 activity in healthy volunteers [J].
Kortunay, S ;
Bozkurt, A ;
Basci, NE ;
Kayaalp, SO .
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 2002, 27 (03) :171-174
[9]
Interindividual variability in inhibition and induction of cytochrome P450 enzymes [J].
Lin, JH ;
Lu, AYH .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :535-567
[10]
LIFE THREATENING INTERACTION BETWEEN TAMOXIFEN AND WARFARIN [J].
LODWICK, R ;
MCCONKEY, B ;
BROWN, AM ;
BEELEY, L .
BRITISH MEDICAL JOURNAL, 1987, 295 (6606) :1141-1141