Detection of cytochrome P450 mRNA transcripts in prostate samples by RT-PCR

被引:66
作者
Finnström, N
Bjelfman, C
Söderström, TG
Smith, G
Egevad, L
Norlén, BJ
Wolf, CR
Rane, A
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Med Lab Sci & Technol, S-14186 Stockholm, Sweden
[2] Univ Uppsala Hosp, Dept Med Sci, S-75185 Uppsala, Sweden
[3] Univ Dundee, Ninewells Hosp & Med Sch, Imperial Canc Res Fund, Mol Pharmacol Unit,Biomed Res Ctr, Dundee DD1 9SY, Scotland
[4] Karolinska Hosp, Dept Pathol & Cytol, S-17176 Stockholm, Sweden
[5] Univ Uppsala Hosp, Dept Surg, S-75185 Uppsala, Sweden
关键词
cytochrome P450; gene expression; prostate; multiplex; reverse transcriptase PCR;
D O I
10.1046/j.1365-2362.2001.00893.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The expression of cytochrome P450 (CYP)-dependent mono-oxygenases in the prostate is important, as it will determine the rate of activation of potential carcinogens as well as the metabolism of hormones with implications in diseases of the prostate. In addition, the levels of cytochromes P450 in prostatic tumours may well be determinants of the outcome of therapy involving P450 substrates such as anti-androgens. Methods The gene expression of 12 different CYP genes was measured by reverse transcription-polymerase chain reaction (RT-PCR) in a total of 28 human prostatic tumour and nontumour samples. Results Intriguingly, a large number of CYP mRNAs were detected in the prostate samples, including CYP1A2, -1B1, -2C19, -2D6, -3A4, -3A5, -3A7 and -4B1. CYP1B1 was consistently expressed and CYP3A5 and CYP4B1 were expressed in a majority of the samples tested. Conclusions These data demonstrate a wide range of CYP genes being expressed in the prostate. The relative importance of these enzymes in the pathogenesis and treatment of prostatic disease remains an important theme for further study.
引用
收藏
页码:880 / 886
页数:7
相关论文
共 36 条
  • [1] [Anonymous], METHOD ENZYMOL
  • [2] Cytochrome P450 1B1:: A major P450 isoenzyme in human blood monocytes and macrophage subsets
    Baron, JM
    Zwadlo-Klarwasser, G
    Jugert, F
    Hamann, W
    Rübben, A
    Mukhtar, H
    Merk, HF
    [J]. BIOCHEMICAL PHARMACOLOGY, 1998, 56 (09) : 1105 - 1110
  • [3] Gene expression of a novel cytochrome P450 of the CYP4F subfamily in human seminal vesicles
    Bylund, J
    Finnström, N
    Oliw, EH
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 261 (01) : 169 - 174
  • [4] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [5] Dassi C, 1998, CLIN CHEM, V44, P2416
  • [6] PROSTATIC-CANCER - AN OVERVIEW
    DENIS, L
    MAHLER, C
    [J]. ACTA ONCOLOGICA, 1990, 29 (05) : 665 - 677
  • [7] STEROIDS AND THE PROSTATE
    EATON, CL
    DAVIES, P
    HARPER, M
    FRANCE, T
    RUSHMERE, N
    GRIFFITHS, K
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (1-3) : 175 - 183
  • [8] PREDICTION OF PROGNOSIS FOR PROSTATIC ADENOCARCINOMA BY COMBINED HISTOLOGICAL GRADING AND CLINICAL STAGING
    GLEASON, DF
    MELLINGE.GT
    [J]. JOURNAL OF UROLOGY, 1974, 111 (01) : 58 - 64
  • [9] Cytochromes P450 .6. Constitutive expression of hepatic cytochrome P450 genes
    Gonzalez, FJ
    Lee, YH
    [J]. FASEB JOURNAL, 1996, 10 (10) : 1112 - 1117
  • [10] MOLECULAR-GENETICS OF THE P-450 SUPERFAMILY
    GONZALEZ, FJ
    [J]. PHARMACOLOGY & THERAPEUTICS, 1990, 45 (01) : 1 - 38