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Identification of miRNAs Differentially Expressed in Prostatic Secretions of Patients with Prostate Cancer

dc.contributor.author Guzel, Esra
dc.contributor.author Karatas, Omer F.
dc.contributor.author Semercioz, Atilla
dc.contributor.author Ekici, Sinan
dc.contributor.author Aykan, Serdar
dc.contributor.author Yentur, Serhat
dc.contributor.author Ozen, Mustafa
dc.date.accessioned 2026-03-26T14:49:42Z
dc.date.available 2026-03-26T14:49:42Z
dc.date.issued 2015
dc.description Semerciöz, Atilla/0000-0001-8688-4772; Ozen, Mustafa/0000-0002-6142-5294; Guzel Tanoglu, Esra/0000-0002-0909-8935; Karatas, Omer/0000-0002-0379-2088 en_US
dc.description.abstract Prostate cancer (PCa) is one of the leading causes of cancer deaths in men. Since there are limited treatment options available for the advanced tumors, there is an urgent need for novel diagnostic tools for PCa. Prostate secretion samples (PSS) from 23 PCa and 25 benign prostate hyperplasia (BPH) patients were obtained from Urology Department of Bagcilar Educational and Research Hospital (Istanbul). MicroRNA (miRNA) profiling of eight PSS (four from BPH, four from PCa patients) was performed using microarray. Four of significantly deregulated miRNAs were further confirmed using quantitative reverse-transcription PCR (qRT-PCR). Statistical analysis was performed using Student's t-test. ROC curves were plotted with SPSS-15.0. In this study, we aimed to identify a miRNA expression signature that could be used to distinguish PCa from BPH. MiRNA profiling of four PCa and four BPH patients with microarray revealed that miR-361-3p, miR-133b and miR-221 were significantly downregulated and miR-203 was upregulated in PSS of PCa patients. Further qRT-PCR analysis confirmed the altered expressions of these four miRNAs in PSS of 23 PCa and 25 BPH patients. Four miRNAs, together and individually have much power (AUC; 0.950) than PSA has (AUC; 0.463) to discriminate PCa from BPH patients. We have shown for the first time in the literature the presence of miRNAs in the PSS. We suggest PSS as a powerful non-invasive source for evaluation of prognosis in PCa, since prostate massages can be easily applied during routine examination. Our results showed that certain differentially expressed miRNAs in PSS could be used as diagnostics markers. What's new? The association of microRNAs (miRNAs) with cancer initiation, progression, and metastasis has fueled increasing interest in their potential as diagnostic and therapeutic markers. The current study aimed to identify an miRNA expression signature that could be used to distinguish prostate cancer from benign prostatic hyperplasia by using prostate secretions obtained from patients. MiRNAs were found to be present in the prostate secretion samples, with altered expression detected for four miRNAs in particular. The findings suggest that certain miRNAs may be powerful tools for aiding prostate cancer diagnosis. en_US
dc.description.sponsorship Scientific Research Projects of Istanbul University [21092]; The Scientific and Technological Research Council of Turkey (TUBITAK) [108S051] en_US
dc.description.sponsorship Grant sponsor: Scientific Research Projects of Istanbul University; Grant number: 21092; Grant sponsor: The Scientific and Technological Research Council of Turkey (TUBITAK); Grant number: 108S051 en_US
dc.identifier.doi 10.1002/ijc.29054
dc.identifier.issn 0020-7136
dc.identifier.issn 1097-0215
dc.identifier.scopus 2-s2.0-84918827158
dc.identifier.uri https://doi.org/10.1002/ijc.29054
dc.identifier.uri https://hdl.handle.net/20.500.14901/2256
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.relation.ispartof International Journal of Cancer en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Benign Prostatic Hyperplasia en_US
dc.subject Diagnostic Biomarkers en_US
dc.subject Microrna en_US
dc.subject Prostate Cancer en_US
dc.title Identification of miRNAs Differentially Expressed in Prostatic Secretions of Patients with Prostate Cancer en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Semerciöz, Atilla/0000-0001-8688-4772
gdc.author.id Ozen, Mustafa/0000-0002-6142-5294
gdc.author.id Guzel Tanoglu, Esra/0000-0002-0909-8935
gdc.author.id Karatas, Omer/0000-0002-0379-2088
gdc.author.scopusid 14119778500
gdc.author.scopusid 36914888500
gdc.author.scopusid 6602236477
gdc.author.scopusid 6603735990
gdc.author.scopusid 56122768100
gdc.author.scopusid 44062076400
gdc.author.scopusid 7004507505
gdc.author.wosid Semerciöz, Atilla/Abg-6597-2020
gdc.author.wosid Ekici, Sinan/Gxz-6673-2022
gdc.author.wosid Ozen, Mustafa/Aet-5367-2022
gdc.author.wosid Guzel Tanoglu, Esra/Aab-8509-2019
gdc.author.wosid Karatas, Omer/I-5103-2013
gdc.description.department Erzurum Technical University en_US
gdc.description.departmenttemp [Guzel, Esra; Karatas, Omer F.; Ozen, Mustafa] Istanbul Univ, Dept Med Genet, Cerrahpasa Med Sch, Istanbul, Turkey; [Guzel, Esra; Ozen, Mustafa] Biruni Univ, Dept Mol Biol & Genet, Istanbul, Turkey; [Karatas, Omer F.] Erzurum Tech Univ, Mol Biol & Genet Dept, Erzurum, Turkey; [Semercioz, Atilla; Aykan, Serdar; Yentur, Serhat] Bagcilar Educ & Res Hosp, Dept Urol, Istanbul, Turkey; [Ekici, Sinan] Maltepe Univ, Dept Urol, Istanbul, Turkey; [Creighton, Chad J.] Baylor Coll Med, Div Biostat, Houston, TX 77030 USA; [Ittmann, Michael; Ozen, Mustafa] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA; [Ittmann, Michael; Ozen, Mustafa] Michael E DeBakey VAMC, Houston, TX USA en_US
gdc.description.endpage 879 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 875 en_US
gdc.description.volume 136 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q1
gdc.identifier.pmid 24976077
gdc.identifier.wos WOS:000346089900034
gdc.virtual.author Karataş, Ömer Faruk
relation.isAuthorOfPublication 03b9f635-74c8-4a6e-adf1-e41b4c4d35d4
relation.isAuthorOfPublication.latestForDiscovery 03b9f635-74c8-4a6e-adf1-e41b4c4d35d4

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