The association of let-7c, miR-21, miR-145, miR-182, and miR-221 with clinicopathologic parameters of prostate cancer in patients diagnosed with low-risk disease

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Background: The diagnostic benefit of prostate specific antigen (PSA) is limited, owing to its lack of specificity, particularly in men with PSA levels of 4.0 to 10.0 ng/mL. Therefore, there is a need for more specific and sensitive biomarkers to improve diagnostic accuracy and to predict prostate cancer (PCa) progression. Assessing the expression levels of specific microRNAs (miRNAs) in patients with PCa may be helpful in detecting cancer and predicting the cancer prognosis and its evolution, and may serve as markers to decide the treatment. We examined the expression levels of five miRNAs (let-7c, miR-21, miR-145, miR-185, and miR-221) on patients with low-risk PCa who had been eligible for active surveillance but underwent radical prostatectomy. We investigated the correlation between the relative expression of miRNAs and clinicopathologic parameters to evaluate their clinical significance. Materials and Methods: Total RNA was isolated from the tumor and the corresponding non-neoplastic prostate tissue of 45 patients who underwent radical prostatectomy. Quantitative reverse transcriptase-polymerase chain reaction was used to measure the levels of let-7c, miR-21, miR-145, miR-185, miR-221, and RNU6B expression, using TaqMan MicroRNA Assays. miRNA expression was examined in low-risk PCa, and miRNAs' association with Gleason upgraded (GU) and biochemical recurrent (BR) patients was evaluated. Results: We observed that miR-21 and miR-182 were overexpressed; conversely, let-7c, miR-145, and miR-221 were underexpressed in patients with low-risk PCa. GU patients (n = 16) and non-upgraded patients (n = 28) were compared. miR-145 was downregulated significantly in the GU group (P = 0.03). Similarly, miR-221 was downregulated significantly in patients with BR (n = 14) compared with non-recurrent patients (n = 30) (P = 0.04). Receiver operator characteristics (ROC) curve analysis revealed that miR-221 levels were significantly associated with BR in patients with a cut-off <−1.666, a value at which sensitivity was 70% and specificity 71% (area under curve [AUC] = 0.705, P = 0.030). Conclusions: There is still a need for a tumor marker with higher sensitivity and specificity than that of PSA. Among the five miRNAs examined, miR-221 was most associated with biochemical recurrence in low-risk PCa. © 2019 Wiley Periodicals, Inc.

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https://rdlopen.rawdatalibrary.net/r/ebyu/13733Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/pros.23825Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKurul, N. Ozgur
dc.contributor.authorAtes, Ferhat
dc.contributor.authorYilmaz, Ismail
dc.contributor.authorNarli, Gizem
dc.contributor.authorYesildal, Cumhur
dc.contributor.authorSenkul, Temucin
dc.date.accessioned2026-10-18T20:28:33.445931985Z
dc.date.available2026-10-18T20:28:33.445931985Z
dc.date.issued2019
dc.description.abstractBackground: The diagnostic benefit of prostate specific antigen (PSA) is limited, owing to its lack of specificity, particularly in men with PSA levels of 4.0 to 10.0 ng/mL. Therefore, there is a need for more specific and sensitive biomarkers to improve diagnostic accuracy and to predict prostate cancer (PCa) progression. Assessing the expression levels of specific microRNAs (miRNAs) in patients with PCa may be helpful in detecting cancer and predicting the cancer prognosis and its evolution, and may serve as markers to decide the treatment. We examined the expression levels of five miRNAs (let-7c, miR-21, miR-145, miR-185, and miR-221) on patients with low-risk PCa who had been eligible for active surveillance but underwent radical prostatectomy. We investigated the correlation between the relative expression of miRNAs and clinicopathologic parameters to evaluate their clinical significance. Materials and Methods: Total RNA was isolated from the tumor and the corresponding non-neoplastic prostate tissue of 45 patients who underwent radical prostatectomy. Quantitative reverse transcriptase-polymerase chain reaction was used to measure the levels of let-7c, miR-21, miR-145, miR-185, miR-221, and RNU6B expression, using TaqMan MicroRNA Assays. miRNA expression was examined in low-risk PCa, and miRNAs' association with Gleason upgraded (GU) and biochemical recurrent (BR) patients was evaluated. Results: We observed that miR-21 and miR-182 were overexpressed; conversely, let-7c, miR-145, and miR-221 were underexpressed in patients with low-risk PCa. GU patients (n = 16) and non-upgraded patients (n = 28) were compared. miR-145 was downregulated significantly in the GU group (P = 0.03). Similarly, miR-221 was downregulated significantly in patients with BR (n = 14) compared with non-recurrent patients (n = 30) (P = 0.04). Receiver operator characteristics (ROC) curve analysis revealed that miR-221 levels were significantly associated with BR in patients with a cut-off <−1.666, a value at which sensitivity was 70% and specificity 71% (area under curve [AUC] = 0.705, P = 0.030). Conclusions: There is still a need for a tumor marker with higher sensitivity and specificity than that of PSA. Among the five miRNAs examined, miR-221 was most associated with biochemical recurrence in low-risk PCa. © 2019 Wiley Periodicals, Inc.
dc.identifier.doi10.1002/pros.23825
dc.identifier.endpage1132
dc.identifier.issn0270-4137
dc.identifier.issue10
dc.identifier.pmid31045265
dc.identifier.scopus2-s2.0-85066398598
dc.identifier.startpage1125
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13733
dc.identifier.volume79
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc.
dc.relation.ispartofProstate
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectlow-risk PCa
dc.subjectmicroRNA
dc.subjectmiRNA
dc.subjectprostate cancer
dc.subjectPSA
dc.subjectAged
dc.subjectBiomarkers, Tumor
dc.subjectGene Expression Regulation, Neoplastic
dc.subjectHumans
dc.subjectMale
dc.subjectMicroRNAs
dc.subjectMiddle Aged
dc.subjectProstate
dc.subjectProstatectomy
dc.subjectProstatic Neoplasms
dc.subjectRetrospective Studies
dc.subjectbiological marker
dc.subjectlet 7c
dc.subjectmicroRNA 145
dc.subjectmicroRNA 182
dc.subjectmicroRNA 21
dc.subjectmicroRNA 221
dc.subjectprostate specific antigen
dc.subjectRNU6B protein
dc.subjectunclassified drug
dc.subjectMIRN145 microRNA, human
dc.subjectMirn182 microRNA, human
dc.subjectMIRN21 microRNA, human
dc.subjectMIRN221 microRNA, human
dc.subjectmirnlet7 microRNA, human
dc.titleThe association of let-7c, miR-21, miR-145, miR-182, and miR-221 with clinicopathologic parameters of prostate cancer in patients diagnosed with low-risk disease
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus26
rdl.source.indexSCOPUS