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Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer

Fucosylation is an important oligosaccharide modification associated with cancer and inflammation. We investigated whether urinary fucosylated PSA (Fuc-PSA) levels could be used for the detection of high Gleason score prostate cancer. Urine samples were collected from men with abnormal digital recta...

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Autores principales: Fujita, Kazutoshi, Hayashi, Takuji, Matsuzaki, Kyosuke, Nakata, Wataru, Masuda, Mika, Kawashima, Atsunari, Ujike, Takeshi, Nagahara, Akira, Tsuchiya, Mutsumi, Kobayashi, Yuka, Nojima, Satoshi, Uemura, Motohide, Morii, Eiichi, Miyoshi, Eiji, Nonomura, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302941/
https://www.ncbi.nlm.nih.gov/pubmed/27494861
http://dx.doi.org/10.18632/oncotarget.10987
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author Fujita, Kazutoshi
Hayashi, Takuji
Matsuzaki, Kyosuke
Nakata, Wataru
Masuda, Mika
Kawashima, Atsunari
Ujike, Takeshi
Nagahara, Akira
Tsuchiya, Mutsumi
Kobayashi, Yuka
Nojima, Satoshi
Uemura, Motohide
Morii, Eiichi
Miyoshi, Eiji
Nonomura, Norio
author_facet Fujita, Kazutoshi
Hayashi, Takuji
Matsuzaki, Kyosuke
Nakata, Wataru
Masuda, Mika
Kawashima, Atsunari
Ujike, Takeshi
Nagahara, Akira
Tsuchiya, Mutsumi
Kobayashi, Yuka
Nojima, Satoshi
Uemura, Motohide
Morii, Eiichi
Miyoshi, Eiji
Nonomura, Norio
author_sort Fujita, Kazutoshi
collection PubMed
description Fucosylation is an important oligosaccharide modification associated with cancer and inflammation. We investigated whether urinary fucosylated PSA (Fuc-PSA) levels could be used for the detection of high Gleason score prostate cancer. Urine samples were collected from men with abnormal digital rectal examination findings or elevated serum PSA levels, before prostate biopsy. Lectin-antibody ELISA was used to quantify the Lewis-type or core-type fucosylated PSA (PSA-AAL) and core-type fucosylated PSA (PSA-PhoSL) in the urine samples. Both types of urinary Fuc-PSA were significantly decreased in the men with prostate cancer compared with the men whose biopsies were negative for cancer (P = 0.026 and P < 0.001, respectively). Both were also significantly associated with the Gleason scores of the biopsy specimens (P = 0.001 and P < 0.001, respectively). Multivariate analysis showed that PSA density, urinary PSA-AAL, and urinary PSA-PhoSL were independent predictors of high Gleason score prostate cancer. The area under the receiver-operator characteristic curve (AUC) value for the prediction of cancers of Gleason score ≥ 7 was 0.69 for urinary PSA-AAL and 0.72 for urinary PSA-PhoSL. In contrast, the AUC value was 0.59 for serum PSA, 0.63 for PSA density, and 0.58 for urinary PSA. In conclusion, a decreased urinary Fuc-PSA level is a potential marker for the detection of high Gleason score prostate cancer.
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spelling pubmed-53029412017-02-13 Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer Fujita, Kazutoshi Hayashi, Takuji Matsuzaki, Kyosuke Nakata, Wataru Masuda, Mika Kawashima, Atsunari Ujike, Takeshi Nagahara, Akira Tsuchiya, Mutsumi Kobayashi, Yuka Nojima, Satoshi Uemura, Motohide Morii, Eiichi Miyoshi, Eiji Nonomura, Norio Oncotarget Research Paper Fucosylation is an important oligosaccharide modification associated with cancer and inflammation. We investigated whether urinary fucosylated PSA (Fuc-PSA) levels could be used for the detection of high Gleason score prostate cancer. Urine samples were collected from men with abnormal digital rectal examination findings or elevated serum PSA levels, before prostate biopsy. Lectin-antibody ELISA was used to quantify the Lewis-type or core-type fucosylated PSA (PSA-AAL) and core-type fucosylated PSA (PSA-PhoSL) in the urine samples. Both types of urinary Fuc-PSA were significantly decreased in the men with prostate cancer compared with the men whose biopsies were negative for cancer (P = 0.026 and P < 0.001, respectively). Both were also significantly associated with the Gleason scores of the biopsy specimens (P = 0.001 and P < 0.001, respectively). Multivariate analysis showed that PSA density, urinary PSA-AAL, and urinary PSA-PhoSL were independent predictors of high Gleason score prostate cancer. The area under the receiver-operator characteristic curve (AUC) value for the prediction of cancers of Gleason score ≥ 7 was 0.69 for urinary PSA-AAL and 0.72 for urinary PSA-PhoSL. In contrast, the AUC value was 0.59 for serum PSA, 0.63 for PSA density, and 0.58 for urinary PSA. In conclusion, a decreased urinary Fuc-PSA level is a potential marker for the detection of high Gleason score prostate cancer. Impact Journals LLC 2016-08-01 /pmc/articles/PMC5302941/ /pubmed/27494861 http://dx.doi.org/10.18632/oncotarget.10987 Text en Copyright: © 2016 Fujita et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Fujita, Kazutoshi
Hayashi, Takuji
Matsuzaki, Kyosuke
Nakata, Wataru
Masuda, Mika
Kawashima, Atsunari
Ujike, Takeshi
Nagahara, Akira
Tsuchiya, Mutsumi
Kobayashi, Yuka
Nojima, Satoshi
Uemura, Motohide
Morii, Eiichi
Miyoshi, Eiji
Nonomura, Norio
Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title_full Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title_fullStr Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title_full_unstemmed Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title_short Decreased fucosylated PSA as a urinary marker for high Gleason score prostate cancer
title_sort decreased fucosylated psa as a urinary marker for high gleason score prostate cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302941/
https://www.ncbi.nlm.nih.gov/pubmed/27494861
http://dx.doi.org/10.18632/oncotarget.10987
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