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Diagnostic biomarkers of prostate cancer

Häggarth, Lars (författare)
Karolinska Institutet, Stockholm
Hägglöf, Christina (författare)
Karolinska Institutet
Jaraj, Sara Jonmarker (författare)
Karolinska Institutet, Stockholm
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Wester, Kenneth (författare)
Uppsala universitet,Molekylär och morfologisk patologi,Forskargrupp Pontén,Akademiska Hospital, Uppsala
Pontén, Fredrik (författare)
Uppsala universitet,Molekylär och morfologisk patologi,Forskargrupp Pontén,Karolinska Institutet, Stockholm och Akademiska Hospital, Uppsala
Östman, Arne (författare)
Karolinska Institutet
Egevad, Lars (författare)
Karolinska Institutet
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 (creator_code:org_t)
2010-11-01
2011
Engelska.
Ingår i: Scandinavian Journal of Urology and Nephrology. - : Informa UK Limited. - 0036-5599 .- 1651-2065. ; 45:1, s. 60-67
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Objective. Diagnostic tissue biomarkers for prostate cancer (PC) include basal cell markers and alpha-methylacyl-coenzyme A-racemase (AMACR), often used in combination. Their sensitivity and specificity are not perfect and there is a need for additional diagnostic biomarkers for PC in cases that are difficult to diagnose on routine stained sections. Material and methods. This study investigated the diagnostic accuracy of three novel tissue biomarkers for PC found through a search in the Human Protein Atlas database (www.proteinatlas.com): somatic cytochrome c (CYCS), intestinal cell kinase (ICK) and inhibitor of nuclear factor-kappa B kinase subunit beta (IKBKB), and compared the results with AMACR. A tissue microarray was constructed from 40 consecutive radical prostatectomy (RP) specimens including benign prostatic tissue, atrophy, high-grade prostatic intraepithelial neoplasia (HGPIN) and PC. Immunoreactivity was scored based on staining intensity and extent. Real-time polymerase chain reaction (PCR) was performed on malignant and benign frozen tissue samples from 32 RP specimens. Results. All four biomarkers showed a stronger expression in PC and HGPIN than in benign tissue (p < 0.001). The highest diagnostic accuracy for PC was achieved with ICK and AMACR at 97%. The area under the curve for CYCS, ICK, IKBKB and AMACR was 0.859, 0.997, 0.865 and 0.983, respectively. The presence of mRNA transcripts of the genes was confirmed by real-time PCR in benign and malignant prostatic tissue. Conclusions. AMACR is an accurate diagnostic tissue marker for PC. However, in some PCs AMACR is false negative and a panel of CYCS, ICK and IKBKB may serve as ancillary diagnostic tool.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

AMACR
cytochrome c
ICK
IKBKB
immunohistochemistry
prostate
prostate cancer
tissue microarray
MEDICINE
MEDICIN

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