Detection of TMPRSS2-ERG fusion transcripts and prostate cancer antigen 3 in urinary sediments may improve diagnosis of prostate cancer

被引:262
作者
Hessels, Daphne
Smit, Frank P.
Verhaegh, Gerald W.
Witjes, J. Alfred
Cornel, Erik B.
Schalken, Jack A.
机构
[1] Radboud Univ Nijmegen Med Ctr, Nijmegen Ctr Mol Life Sci Internal Postal Code 26, NL-6500 HB Nijmegen, Netherlands
[2] Twente Hosp Grp, Dept Urol, Hengelo, Netherlands
关键词
D O I
10.1158/1078-0432.CCR-07-0700
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Early detection of prostate cancer can increase the curative success rate for prostate cancer. We studied the diagnostic usefulness of TMPRSS2-ERG fusion transcripts as well as the combination of prostate cancer antigen 3 (PCA3) RNA and TMPRSS2-ERG fusion transcripts in urinary sediments after digital rectal examination (DRE). Experimental Design: A total of 78 men with prostate cancer - positive biopsies and 30 men with prostate cancer-negative biopsies were included in this study. After DRE, the first voided urine was collected, and urinary sediments were obtained. We used semiquantitative reverse transcription-PCR (RT-PCR) analysis followed by Southern blot hybridization with a radiolabeled probe for the detection TMPRSS2-ERG fusion transcripts in these urinary sediments. A quantitative RT-PCR assay for PCA3 was used to determine the PCA3 score in the same sediments. Results: TMPRSS2-ERG fusion transcripts can be detected in the urine after DRE with a sensitivity of 37%. In this cohort of patients, the PCA3-based assay had a sensitivity of 62%. When both markers were combined, the sensitivity increased to 73%. Especially in the cohort of men with persistently elevated serum prostate-specific antigen levels and history of negative biopsies, the high positive predictive value of 94% of TMPRSS2-ERG fusion transcripts could give a better indication which patients require repeat biopsies. Conclusion: In this report, we used for the first time the combination of the prostate cancer specific biomarkers TMPRSS2-ERG and PCA3, which significantly improves the sensitivity for prostate cancer diagnosis.
引用
收藏
页码:5103 / 5108
页数:6
相关论文
共 21 条
[1]  
Bussemakers MJG, 1999, CANCER RES, V59, P5975
[2]   TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesions [J].
Cerveira, Nuno ;
Ribeiro, Franclim R. ;
Peixoto, Ana ;
Costa, Vera ;
Henrique, Rui ;
Jeronimo, Carmen ;
Teixeira, Manuel R. .
NEOPLASIA, 2006, 8 (10) :826-832
[3]  
Church K. W., 1991, Computer Speech and Language, V5, P19, DOI 10.1016/0885-2308(91)90016-J
[4]   Diversity of TMPRSS2-ERG fusion transcripts in the human prostate [J].
Clark, J. ;
Merson, S. ;
Jhavar, S. ;
Flohr, P. ;
Edwards, S. ;
Foster, C. S. ;
Eeles, R. ;
Martin, F. L. ;
Phillips, D. H. ;
Crundwell, M. ;
Christmas, T. ;
Thompson, A. ;
Fisher, C. ;
Kovacs, G. ;
Cooper, C. S. .
ONCOGENE, 2007, 26 (18) :2667-2673
[5]  
de Kok JB, 2002, CANCER RES, V62, P2695
[6]  
DEMICHELIS F, 2007, ONCOGENE
[7]   uPM3, a new molecular urine test for the detection of prostate cancer [J].
Fradet, YF ;
Saad, F ;
Aprikian, A ;
Dessureault, J ;
Elhilali, M ;
Trudel, C ;
Måsse, B ;
Piché, L ;
Chypre, C .
UROLOGY, 2004, 64 (02) :311-315
[8]   DD3PCA3-based molecular urine analysis for the diagnosis of prostate cancer [J].
Hessels, D ;
Gunnewiek, JMTK ;
van Oort, I ;
Karthaus, HFM ;
van Leenders, GJL ;
van Balken, B ;
Kiemeney, LA ;
Witjes, JA ;
Schalken, JA .
EUROPEAN UROLOGY, 2003, 44 (01) :8-15
[9]   Applicability of biomarkers in the early diagnosis of prostate cancer [J].
Hessels, D ;
Verhaegh, GW ;
Schalken, JA ;
Witjes, JA .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2004, 4 (04) :513-526
[10]   Cancer statistics, 2007 [J].
Jemal, Ahmedin ;
Siegel, Rebecca ;
Ward, Elizabeth ;
Murray, Taylor ;
Xu, Jiaquan ;
Thun, Michael J. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2007, 57 (01) :43-66