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Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer

The aim of this study is to elucidate the clinical significance of prostate-specific membrane antigen (PSMA) expression in circulating tumor cells (CTCs) from castration-resistant prostate cancer (CRPC) patients. We analyzed a total of 203 CTC samples from 79 CRPC patients to investigate the proport...

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Autores principales: Nagaya, Naoya, Nagata, Masayoshi, Lu, Yan, Kanayama, Mayuko, Hou, Qi, Hotta, Zen-u, China, Toshiyuki, Kitamura, Kosuke, Matsushita, Kazuhito, Isotani, Shuji, Muto, Satoru, Sakamoto, Yoshiro, Horie, Shigeo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984691/
https://www.ncbi.nlm.nih.gov/pubmed/31986176
http://dx.doi.org/10.1371/journal.pone.0226219
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author Nagaya, Naoya
Nagata, Masayoshi
Lu, Yan
Kanayama, Mayuko
Hou, Qi
Hotta, Zen-u
China, Toshiyuki
Kitamura, Kosuke
Matsushita, Kazuhito
Isotani, Shuji
Muto, Satoru
Sakamoto, Yoshiro
Horie, Shigeo
author_facet Nagaya, Naoya
Nagata, Masayoshi
Lu, Yan
Kanayama, Mayuko
Hou, Qi
Hotta, Zen-u
China, Toshiyuki
Kitamura, Kosuke
Matsushita, Kazuhito
Isotani, Shuji
Muto, Satoru
Sakamoto, Yoshiro
Horie, Shigeo
author_sort Nagaya, Naoya
collection PubMed
description The aim of this study is to elucidate the clinical significance of prostate-specific membrane antigen (PSMA) expression in circulating tumor cells (CTCs) from castration-resistant prostate cancer (CRPC) patients. We analyzed a total of 203 CTC samples from 79 CRPC patients to investigate the proportion of positive mRNA expressions at different treatment phases. Among them, we elected to focus on specimens from 56 CRPC patients who progressed on therapy and were subsequently provided a new treatment (treatment-switch cohort). In this cohort, we investigated the association between PSMA expression in CTCs and treatment response. CTCs were detected in 55/79 patients and median serum PSA in CTC-positive patients was 67.0 ng/ml. In the treatment-switch cohort of 56 patients, 20 patients were positive for PSMA in CTCs. PSMA expression was inversely associated with percentage of change in prostate-specific antigen (PSA). The median PSA progression-free survival and overall survival were significantly shorter in the PSMA-positive cohort. Furthermore, PSMA expression was predictive of poorer treatment response, shorter PSA progression-free survival and overall survival. PSMA expression in circulating tumor cells may be a novel poor prognostic marker for CRPC.
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spelling pubmed-69846912020-02-07 Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer Nagaya, Naoya Nagata, Masayoshi Lu, Yan Kanayama, Mayuko Hou, Qi Hotta, Zen-u China, Toshiyuki Kitamura, Kosuke Matsushita, Kazuhito Isotani, Shuji Muto, Satoru Sakamoto, Yoshiro Horie, Shigeo PLoS One Research Article The aim of this study is to elucidate the clinical significance of prostate-specific membrane antigen (PSMA) expression in circulating tumor cells (CTCs) from castration-resistant prostate cancer (CRPC) patients. We analyzed a total of 203 CTC samples from 79 CRPC patients to investigate the proportion of positive mRNA expressions at different treatment phases. Among them, we elected to focus on specimens from 56 CRPC patients who progressed on therapy and were subsequently provided a new treatment (treatment-switch cohort). In this cohort, we investigated the association between PSMA expression in CTCs and treatment response. CTCs were detected in 55/79 patients and median serum PSA in CTC-positive patients was 67.0 ng/ml. In the treatment-switch cohort of 56 patients, 20 patients were positive for PSMA in CTCs. PSMA expression was inversely associated with percentage of change in prostate-specific antigen (PSA). The median PSA progression-free survival and overall survival were significantly shorter in the PSMA-positive cohort. Furthermore, PSMA expression was predictive of poorer treatment response, shorter PSA progression-free survival and overall survival. PSMA expression in circulating tumor cells may be a novel poor prognostic marker for CRPC. Public Library of Science 2020-01-27 /pmc/articles/PMC6984691/ /pubmed/31986176 http://dx.doi.org/10.1371/journal.pone.0226219 Text en © 2020 Nagaya et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Nagaya, Naoya
Nagata, Masayoshi
Lu, Yan
Kanayama, Mayuko
Hou, Qi
Hotta, Zen-u
China, Toshiyuki
Kitamura, Kosuke
Matsushita, Kazuhito
Isotani, Shuji
Muto, Satoru
Sakamoto, Yoshiro
Horie, Shigeo
Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title_full Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title_fullStr Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title_full_unstemmed Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title_short Prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
title_sort prostate-specific membrane antigen in circulating tumor cells is a new poor prognostic marker for castration-resistant prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984691/
https://www.ncbi.nlm.nih.gov/pubmed/31986176
http://dx.doi.org/10.1371/journal.pone.0226219
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