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

Abstract 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 t...

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Veröffentlicht in:Urologic oncology 2017-10, Vol.35 (10), p.607.e15-607.e24
Hauptverfasser: Özdemir, Taha Reşid, M.D., Ph.D, Şimşir, Adnan, M.D, Onay, Hüseyin, M.D, Cüreklibatır, İbrahim, M.D, Özkınay, Ferda, M.D, Akın, Haluk, M.D
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Sprache:eng
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Zusammenfassung:Abstract 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.
ISSN:1078-1439
1873-2496
DOI:10.1016/j.urolonc.2017.05.020