• Title of article

    CYP1B1 expression in prostate is higher in the peripheral than in the transition zone

  • Author/Authors

    Ragavan، نويسنده , , Narasimhan and Hewitt، نويسنده , , Rebecca and Cooper، نويسنده , , Leanne J. and Ashton، نويسنده , , Katherine M. and Hindley، نويسنده , , Andrew C. and Nicholson، نويسنده , , Caroline M. and Fullwood، نويسنده , , Nigel J. and Matanhelia، نويسنده , , Shyam S. and Martin، نويسنده , , Francis L.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2004
  • Pages
    10
  • From page
    69
  • To page
    78
  • Abstract
    Prostate cancer (CaP) mostly occurs in the peripheral zone whereas benign prostatic hypertrophy (BPH) occurs in the transition zone. Human prostates (n=12) were obtained, with ethical approval, from radical retropubic prostatectomies. Following resection, tissue sets consisting of peripheral zone and transition zone were isolated from a lobe pre-operatively identified as negative for CaP. Real-time RT-PCR was employed to quantitatively examine CYP1A1, CYP1A2 and CYP1B1. Quantifiable CYP1A1 expression was observed (in nine out of twelve tissue sets) whilst CYP1A2 mRNA transcripts, although detectable (in six out of twelve tissue sets), were unquantifiable. In ten tissue sets, 2- to 6-fold higher CYP1B1 expression in peripheral zone as compared to transition zone was observed. In the other two, equal CYP1B1 expression levels were observed; retrospective examination identified malignancy in one of the zones. Inter-individual variations (up to 10-fold) in CYP1B1 were also noted. Immunohistochemistry for CYP1B1 showed epithelial and stromal nuclear staining. Since CYP1B1 metabolises hormones and carcinogens our results, if confirmed, suggest that this enzyme may influence susceptibility to CaP.
  • Keywords
    Human prostate , Radical retropubic prostatectomy , CYP1B1 , Transition zone , Nuclear staining , Peripheral zone
  • Journal title
    Cancer Letters
  • Serial Year
    2004
  • Journal title
    Cancer Letters
  • Record number

    1807072