Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.

While measurement of serum prostate specific antigen (PSA) is an important screening tool for prostate cancer, new biomarkers are necessary for better discrimination between presence and absence of disease. The MIL-38 monoclonal antibody is specific for the membrane glycoprotein glypican 1 (GPC-1) a...

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Main Authors: Douglas H Campbell, Maria E Lund, Aline L Nocon, Paul J Cozzi, Mark Frydenberg, Paul De Souza, Belinda Schiller, Jennifer L Beebe-Dimmer, Julie J Ruterbusch, Bradley J Walsh
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5908171?pdf=render
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spelling doaj-a299413e192c446ba7d544b767aaa3052020-11-24T22:12:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01134e019601710.1371/journal.pone.0196017Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.Douglas H CampbellMaria E LundAline L NoconPaul J CozziMark FrydenbergPaul De SouzaBelinda SchillerJennifer L Beebe-DimmerJulie J RuterbuschBradley J WalshWhile measurement of serum prostate specific antigen (PSA) is an important screening tool for prostate cancer, new biomarkers are necessary for better discrimination between presence and absence of disease. The MIL-38 monoclonal antibody is specific for the membrane glycoprotein glypican 1 (GPC-1) and binds to prostate cancer tissue. Urine is known to be a source of cellular material. Thus, we hypothesized that detection of GPC-1 in urine cellular material may identify individuals with prostate cancer. Urine samples from patients with prostate cancer, benign prostatic hyperplasia (BPH), or normal controls were collected and cell sediments prepared. GPC-1-positive cells were detected using a MIL-38 immunofluorescence assay (IFA) and samples were classed positive or negative for GPC-1 expressing cells. Assay sensitivity and specificity, stratified by PSA, was reported. A total of 125 patient samples were analyzed (N = 41 prostate cancer; N = 37 BPH; N = 47 normal controls). The use of MIL-38 to detect GPC-1 by IFA discriminated between prostate cancer and BPH urine specimens with a sensitivity and specificity of 71% and 76%, respectively. Assay specificity increased with increasing PSA, with the highest specificity (89%) for patients with PSA ≥4 ng/ml. At lower PSA (<2 ng/ml) specificity decreased, as evidenced by a greater number of false positives in this concentration range. The odds ratio (OR) and 95% confidence intervals (CIs) for GPC-1-positive cells in patients with prostate cancer, adjusted for PSA, was greatest at the lowest serum PSA (<2 ng/ml; OR = 13.4; 95% CI: 4.0-44.7) compared with no adjustment for PSA (OR = 6.4; 95% CI: 2.8-14.9). The use of MIL-38 for detection of GPC-1 may be a useful tool for detection of prostate cancer.http://europepmc.org/articles/PMC5908171?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Douglas H Campbell
Maria E Lund
Aline L Nocon
Paul J Cozzi
Mark Frydenberg
Paul De Souza
Belinda Schiller
Jennifer L Beebe-Dimmer
Julie J Ruterbusch
Bradley J Walsh
spellingShingle Douglas H Campbell
Maria E Lund
Aline L Nocon
Paul J Cozzi
Mark Frydenberg
Paul De Souza
Belinda Schiller
Jennifer L Beebe-Dimmer
Julie J Ruterbusch
Bradley J Walsh
Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
PLoS ONE
author_facet Douglas H Campbell
Maria E Lund
Aline L Nocon
Paul J Cozzi
Mark Frydenberg
Paul De Souza
Belinda Schiller
Jennifer L Beebe-Dimmer
Julie J Ruterbusch
Bradley J Walsh
author_sort Douglas H Campbell
title Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
title_short Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
title_full Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
title_fullStr Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
title_full_unstemmed Detection of glypican-1 (GPC-1) expression in urine cell sediments in prostate cancer.
title_sort detection of glypican-1 (gpc-1) expression in urine cell sediments in prostate cancer.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description While measurement of serum prostate specific antigen (PSA) is an important screening tool for prostate cancer, new biomarkers are necessary for better discrimination between presence and absence of disease. The MIL-38 monoclonal antibody is specific for the membrane glycoprotein glypican 1 (GPC-1) and binds to prostate cancer tissue. Urine is known to be a source of cellular material. Thus, we hypothesized that detection of GPC-1 in urine cellular material may identify individuals with prostate cancer. Urine samples from patients with prostate cancer, benign prostatic hyperplasia (BPH), or normal controls were collected and cell sediments prepared. GPC-1-positive cells were detected using a MIL-38 immunofluorescence assay (IFA) and samples were classed positive or negative for GPC-1 expressing cells. Assay sensitivity and specificity, stratified by PSA, was reported. A total of 125 patient samples were analyzed (N = 41 prostate cancer; N = 37 BPH; N = 47 normal controls). The use of MIL-38 to detect GPC-1 by IFA discriminated between prostate cancer and BPH urine specimens with a sensitivity and specificity of 71% and 76%, respectively. Assay specificity increased with increasing PSA, with the highest specificity (89%) for patients with PSA ≥4 ng/ml. At lower PSA (<2 ng/ml) specificity decreased, as evidenced by a greater number of false positives in this concentration range. The odds ratio (OR) and 95% confidence intervals (CIs) for GPC-1-positive cells in patients with prostate cancer, adjusted for PSA, was greatest at the lowest serum PSA (<2 ng/ml; OR = 13.4; 95% CI: 4.0-44.7) compared with no adjustment for PSA (OR = 6.4; 95% CI: 2.8-14.9). The use of MIL-38 for detection of GPC-1 may be a useful tool for detection of prostate cancer.
url http://europepmc.org/articles/PMC5908171?pdf=render
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