Whole-genome gene expression analysis in urine samples of patients with prostate cancer and benign prostate hyperplasia

被引:4
作者
Ozdemir, Taha Resid [1 ,3 ]
Simsir, Adnan [2 ]
Onay, Huseyin [1 ]
Cureklibatir, Ibrahim [2 ]
Ozkinay, Ferda [1 ]
Akin, Haluk [1 ]
机构
[1] Ege Univ, Dept Med Genet, Fac Med, Izmir, Turkey
[2] Ege Univ, Dept Urol, Fac Med, Izmir, Turkey
[3] Hlth Sci Univ, Izmir Tepecik Training & Res Hosp, Genet Diagnost Ctr, Izmir, Turkey
关键词
Prostate cancer; Biomarker; Gene expression; Microarray; Benign prostate hyperplasia; Urine; BIOMARKERS; PROJECT; MARKERS;
D O I
10.1016/j.urolonc.2017.05.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: There is an urgent need to find new biomarkers with higher specificity and sensitivity for using early detection of prostate cancer (PrCa) and reducing recurrent unnecessary biopsy rates, psychological and physical stress on the patient, and costs. Being noninvasive, urine-based tests might be suitable in routine practice. The aim of this study was to report the first whole-genome gene expression analysis in urine samples, as noninvasive method, that were obtained from PrCa, benign prostate hyperplasia (BPH), and control groups by using the microarray system from Turkey, to our knowledge. Methods: Whole-genome gene expression profiling was conducted in urine samples of 25 patients with PrCa, 24 patients with BPH, and 11 healthy males by using the Illumina Hi Scan microarray system. Results: The number of probes showing a significant change at the level of expression were 101 and 75 in PrCa-control and BPH-control comparison groups, respectively. Further, 51 of them were the same in both comparison groups. There was no significant change at the level of expression in PrCa-BPH comparison group. Conclusion: This study revealed several candidate biomarkers for early diagnosis of PrCa and contributed to the literature by detecting the differences of gene expression profiles in urine samples of PrCa-control and BPH-control comparison groups using the microarray. However, further studies are needed in larger groups. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:607.e15 / 607.e24
页数:10
相关论文
共 22 条
[1]  
Bussemakers MJG, 1999, CANCER RES, V59, P5975
[2]   MEASUREMENT OF PROSTATE-SPECIFIC ANTIGEN IN SERUM AS A SCREENING-TEST FOR PROSTATE-CANCER [J].
CATALONA, WJ ;
SMITH, DS ;
RATLIFF, TL ;
DODDS, KM ;
COPLEN, DE ;
YUAN, JJJ ;
PETROS, JA ;
ANDRIOLE, GL .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (17) :1156-1161
[3]  
de Kok JB, 2002, CANCER RES, V62, P2695
[4]   Characteristic gene expression profiles of benign prostatic hypertrophy and prostate cancer [J].
Endo, Takumi ;
Uzawa, Katsuhiro ;
Suzuki, Hiroyoshi ;
Tanzawa, Hideki ;
Ichikawa, Tomohiko .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2009, 35 (03) :499-509
[5]   Decrease and gain of gene expression are equally discriminatory markers for prostate carcinoma -: A gene expression analysis on total and microdissected prostate tissue [J].
Ernst, T ;
Hergenhahn, M ;
Kenzelmann, M ;
Cohen, CD ;
Bonrouhi, M ;
Weninger, A ;
Klären, R ;
Gröne, EF ;
Wiesel, M ;
Güdemann, C ;
Küster, J ;
Schott, W ;
Staehler, G ;
Kretzler, M ;
Hollstein, M ;
Gröne, HJ .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (06) :2169-2180
[6]   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
[7]   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
[8]   Expression profiling of microdissected matched prostate cancer samples reveals CD166/MEMD and CD24 as new prognostic markers for patient survival [J].
Kristiansen, G ;
Pilarsky, C ;
Wissmann, C ;
Kaiser, S ;
Bruemmendorf, T ;
Roepcke, S ;
Dahl, E ;
Hinzmann, B ;
Specht, T ;
Pervan, J ;
Stephan, C ;
Loening, S ;
Dietel, M ;
Rosenthal, A .
JOURNAL OF PATHOLOGY, 2005, 205 (03) :359-376
[9]  
Luo J, 2001, CANCER RES, V61, P4683
[10]   Gene expression analysis of prostate cancers [J].
Luo, JH ;
Yu, YP ;
Cieply, K ;
Lin, F ;
Deflavia, P ;
Dhir, R ;
Finkelstein, S ;
Michalopoulos, G ;
Becich, M .
MOLECULAR CARCINOGENESIS, 2002, 33 (01) :25-35