A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone

Purpose: The aim of this study was to identify a noninvasive urinary marker for prostate cancer (PCa) diagnosis and to validate the clinical performance of this novel urinary mRNA signature using the droplet digital polymerase chain reaction (ddPCR) approach. Materials and Methods: A gene expression...

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Main Authors: Ho Won Kang, Hee Youn Lee, Young Joon Byun, Pildu Jeong, Jin Sun Yoon, Dong Ho Kim, Won Tae Kim, Yong-June Kim, Sang-Cheol Lee, Seok Joong Yun, Wun-Jae Kim
Format: Article
Language:English
Published: Korean Urological Association 2020-07-01
Series:Investigative and Clinical Urology
Subjects:
Online Access:https://www.icurology.org/Synapse/Data/PDFData/2020ICU/icu-61-411.pdf
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spelling doaj-68df521e69964d9fb3b5762a840a43942020-11-25T03:52:13ZengKorean Urological AssociationInvestigative and Clinical Urology2466-04932466-054X2020-07-0161441141810.4111/icu.2020.61.4.411A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zoneHo Won Kang 0https://orcid.org/0000-0002-8164-4427Hee Youn Lee 1https://orcid.org/0000-0001-8065-2807Young Joon Byun 2https://orcid.org/0000-0003-0528-1502Pildu Jeong 3https://orcid.org/0000-0002-5602-5376Jin Sun Yoon 4https://orcid.org/0000-0002-8442-549XDong Ho Kim 5https://orcid.org/0000-0002-0225-9847Won Tae Kim 6https://orcid.org/0000-0002-7482-4550Yong-June Kim 7https://orcid.org/0000-0001-7638-7174Sang-Cheol Lee8https://orcid.org/0000-0002-4163-2210Seok Joong Yun 9https://orcid.org/0000-0001-7737-4746Wun-Jae Kim 10https://orcid.org/0000-0002-8060-8926Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Molecular Genetics, Bio-Medical Science Co., Ltd., Seoul, Korea.Molecular Genetics, Bio-Medical Science Co., Ltd., Seoul, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Department of Urology, Chungbuk National University Hospital, Chungbuk National University College of Medicine, Cheongju, Korea.Purpose: The aim of this study was to identify a noninvasive urinary marker for prostate cancer (PCa) diagnosis and to validate the clinical performance of this novel urinary mRNA signature using the droplet digital polymerase chain reaction (ddPCR) approach. Materials and Methods: A gene expression microarray (HT-12, Illumina Inc., USA) was used to identify genes differentially expressed between 16 PCa and 8 benign prostatic hyperplasia (BPH) tissues; ddPCR (QX200; Bio-Rad Laboratories, USA) was carried out to quantify the expression of selected genes in urine. The urinary molecular PCa risk score (UMPCaRS) was calculated by using the sum of three upregulated genes as the numerator and the sum of three downregulated genes as the denominator. The diagnostic utility of the UMPCaRS was validated by using a screening set (10 PCa and 10 BPH samples) and a validation set (131 PCa and 105 BPH samples). Results: Three upregulated genes (PDLIM5, GDF-15, THBS4) and three downregulated genes (UPK1A, SSTR3, NPFFR2) were selected from the microarray and subjected to ddPCR. The UMPCaRS for PCa in the screening and validation sets was significantly higher than that for BPH. For the validation set, the diagnostic accuracy of the UMPCaRS was comparable with that of prostate-specific antigen (PSA). Importantly, in the “PSA gray zone” (3–10 ng/mL), the AUC for the UMPCaRS was 0.843 and that for PSA was 0.628 (p<0.001). Conclusions: The data demonstrate that the UMPCaRS is useful for discriminating between PCa and BPH in the “PSA gray zone”.https://www.icurology.org/Synapse/Data/PDFData/2020ICU/icu-61-411.pdfdiagnosismicroarray analysisprostatic neoplasmsurine
collection DOAJ
language English
format Article
sources DOAJ
author Ho Won Kang
Hee Youn Lee
Young Joon Byun
Pildu Jeong
Jin Sun Yoon
Dong Ho Kim
Won Tae Kim
Yong-June Kim
Sang-Cheol Lee
Seok Joong Yun
Wun-Jae Kim
spellingShingle Ho Won Kang
Hee Youn Lee
Young Joon Byun
Pildu Jeong
Jin Sun Yoon
Dong Ho Kim
Won Tae Kim
Yong-June Kim
Sang-Cheol Lee
Seok Joong Yun
Wun-Jae Kim
A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
Investigative and Clinical Urology
diagnosis
microarray analysis
prostatic neoplasms
urine
author_facet Ho Won Kang
Hee Youn Lee
Young Joon Byun
Pildu Jeong
Jin Sun Yoon
Dong Ho Kim
Won Tae Kim
Yong-June Kim
Sang-Cheol Lee
Seok Joong Yun
Wun-Jae Kim
author_sort Ho Won Kang
title A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
title_short A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
title_full A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
title_fullStr A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
title_full_unstemmed A novel urinary mRNA signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
title_sort novel urinary mrna signature using the droplet digital polymerase chain reaction platform improves discrimination between prostate cancer and benign prostatic hyperplasia within the prostate-specific antigen gray zone
publisher Korean Urological Association
series Investigative and Clinical Urology
issn 2466-0493
2466-054X
publishDate 2020-07-01
description Purpose: The aim of this study was to identify a noninvasive urinary marker for prostate cancer (PCa) diagnosis and to validate the clinical performance of this novel urinary mRNA signature using the droplet digital polymerase chain reaction (ddPCR) approach. Materials and Methods: A gene expression microarray (HT-12, Illumina Inc., USA) was used to identify genes differentially expressed between 16 PCa and 8 benign prostatic hyperplasia (BPH) tissues; ddPCR (QX200; Bio-Rad Laboratories, USA) was carried out to quantify the expression of selected genes in urine. The urinary molecular PCa risk score (UMPCaRS) was calculated by using the sum of three upregulated genes as the numerator and the sum of three downregulated genes as the denominator. The diagnostic utility of the UMPCaRS was validated by using a screening set (10 PCa and 10 BPH samples) and a validation set (131 PCa and 105 BPH samples). Results: Three upregulated genes (PDLIM5, GDF-15, THBS4) and three downregulated genes (UPK1A, SSTR3, NPFFR2) were selected from the microarray and subjected to ddPCR. The UMPCaRS for PCa in the screening and validation sets was significantly higher than that for BPH. For the validation set, the diagnostic accuracy of the UMPCaRS was comparable with that of prostate-specific antigen (PSA). Importantly, in the “PSA gray zone” (3–10 ng/mL), the AUC for the UMPCaRS was 0.843 and that for PSA was 0.628 (p<0.001). Conclusions: The data demonstrate that the UMPCaRS is useful for discriminating between PCa and BPH in the “PSA gray zone”.
topic diagnosis
microarray analysis
prostatic neoplasms
urine
url https://www.icurology.org/Synapse/Data/PDFData/2020ICU/icu-61-411.pdf
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