Differential drug-induced mRNA expression of human CYP3A4 compared to CYP3A5, CYP3A7 and CYP3A43

被引:56
|
作者
Krusekopf, S
Roots, I
Kleeberg, U
机构
[1] Humboldt Univ, Charite, Inst Clin Pharmacol, D-10098 Berlin, Germany
[2] Fed Inst Drugs & Med Devices, D-53113 Bonn, Germany
关键词
CYP3A (Cytochrome P450 3A); omeprazole; pantoprazole; St. John's wort; induction of transcription; RT-PCR (reverse transcription-polymerase; chain reaction);
D O I
10.1016/S0014-2999(03)01481-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug-mediated regulation of mRNA expression of all members of the cytochrome P450 3A (CYP3A) subfamily has been measured by reverse transcription - polymerase chain reaction (RT-PCR) in the human hepatocellular carcinoma cell line, HepG2. Transcriptional regulation was proved by inhibition of induction with actinomycin D. Besides the positive control dexamethasone, the H+/K+-ATPase inhibitors omeprazole, lansoprazole, pantoprazole, and rabeprazole, and the herbal antidepressant St. John's wort (Hypericum extract) were studied. All CYP3A mRNAs were induced by dexamethasone. CYP3A4 was the only CYP3A isoform that was induced by all of the four benzimidazole derivatives, while CYP3A5, CYP3A7, and CYP3A43 were unaffected or even slightly downregulated by these drugs. St. John's wort also increased CYP3A4 mRNA exclusively, leaving CYP3A5 and CYP3A43 unaffected, whereas CYP3A7 was decreased. Depending on the inducer, expression of CYP3A4 is differently regulated from CYP3A5, CYP3A7, and CYP3A43. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
相关论文
共 50 条
  • [1] Expression of CYP3A4, CYP3A5 and CYP3A7 in human duodenal tissue
    Kivisto, KT
    Bookjans, G
    Fromm, MF
    Griese, EU
    Munzel, P
    Kroemer, HK
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 42 (03) : 387 - 389
  • [2] Comparative metabolic capabilities of CYP3A4, CYP3A5, and CYP3A7
    Williams, JA
    Ring, BJ
    Cantrell, VE
    Jones, DR
    Eckstein, J
    Ruterbories, K
    Hamman, MA
    Hall, SD
    Wrighton, SA
    DRUG METABOLISM AND DISPOSITION, 2002, 30 (08) : 883 - 891
  • [3] CYP3A4, CYP3A5, and CYP3A43 genotypes and haplotypes in the etiology and severity of prostate cancer
    Zeigler-Johnson, C
    Friebel, T
    Walker, AH
    Wang, YT
    Spangler, E
    Panossian, S
    Patacsil, M
    Aplenc, R
    Wein, AJ
    Malkowicz, SB
    Rebbeck, TR
    CANCER RESEARCH, 2004, 64 (22) : 8461 - 8467
  • [4] SEQUENCE OF THE 5'-FLANKING REGION OF CYP3A5 - COMPARATIVE-ANALYSIS WITH CYP3A4 AND CYP3A7
    JOUNAIDI, Y
    GUZELIAN, PS
    MAUREL, P
    VILAREM, MJ
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (03) : 1741 - 1747
  • [5] Differences in CYP3A4*1G genotype distribution and haplotypes of CYP3A4, CYP3A5 and CYP3A7 in 3 Chinese populations
    Du, Jing
    Yu, Lan
    Wang, Lei
    Zhang, Aiping
    Shi, Yongyong
    Li, Xingwang
    Xing, Qinghe
    He, Lin
    Shu, Anli
    Xu, Lingyun
    Xu, Mingsheng
    Feng, Guoyin
    CLINICA CHIMICA ACTA, 2007, 383 (1-2) : 172 - 174
  • [6] Genetic polymorphisms of the CYP3A4, CYP3A5, CYP3A7 and CYP1A2 among the Jordanian population
    Salameh, Ghada
    Al Hadidi, Kamal
    El Khateeb, Mohammad
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2012, 34 (01) : 23 - 33
  • [7] Effect of five HIV protease inhibitors on CYP3A4, CYP3A5, and CYP3A7 activities in vitro
    Granfors, MT
    Kajosaari, LI
    Wang, JS
    Laitila, J
    Neuvonen, PJ
    Backman, JT
    DRUG METABOLISM REVIEWS, 2003, 35 : 48 - 48
  • [8] Effect of CYP3A5 genotype on the relationship between hepatic CYP3A activity and CYP3A4 and CYP3A5 mRNA expression
    Kolwankar, D
    Ho, H
    Ethell, B
    Vuppalanchi, R
    Marri, SR
    Wrighton, SA
    Jones, DR
    Hall, SD
    DRUG METABOLISM REVIEWS, 2004, 36 : 118 - 118
  • [9] Selective expression of CYP3A5 and not CYP3A4 in human blood
    Janardan, SK
    Lown, KS
    SchmiedlinRen, P
    Thummel, KE
    Watkins, PB
    PHARMACOGENETICS, 1996, 6 (05): : 379 - 385
  • [10] Expression and localization of CYP3A4 and CYP3A5 in human lung
    Anttila, S
    Hukkanen, J
    Hakkola, J
    Stjernvall, T
    Beaune, P
    Edwards, RJ
    Boobis, AR
    Pelkonen, O
    Raunio, H
    AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1997, 16 (03) : 242 - 249