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Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I

Galectin-3 (Gal-3), an oncogenic pro-inflammatory protein, has been suggested as a possible complementary diagnostic candidate to prostate specific antigen (PSA) blood test for prostate cancer patients. The presence of the proteins in the circulation (biomarkers) may elicit an intrinsic humoral immu...

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Autores principales: Nakajima, Kosei, Heilbrun, Lance K, Hogan, Victor, Smith, Daryn, Heath, Elisabeth, Raz, Avraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347690/
https://www.ncbi.nlm.nih.gov/pubmed/27741512
http://dx.doi.org/10.18632/oncotarget.12619
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author Nakajima, Kosei
Heilbrun, Lance K
Hogan, Victor
Smith, Daryn
Heath, Elisabeth
Raz, Avraham
author_facet Nakajima, Kosei
Heilbrun, Lance K
Hogan, Victor
Smith, Daryn
Heath, Elisabeth
Raz, Avraham
author_sort Nakajima, Kosei
collection PubMed
description Galectin-3 (Gal-3), an oncogenic pro-inflammatory protein, has been suggested as a possible complementary diagnostic candidate to prostate specific antigen (PSA) blood test for prostate cancer patients. The presence of the proteins in the circulation (biomarkers) may elicit an intrinsic humoral immune reaction by generating autoantibodies, which consequently could alter the detection levels. Here, we report the associations of the two prostate cancer biomarkers, Gal-3 and PSA in patients at different clinical states of prostate cancer while taking into account the autoantibody levels. A blind, prospective, single institution, pilot study was conducted. A total of 95 men were classified into 5 groups: healthy controls (Group1), newly diagnosed patients (Group2), no recurrence after local therapy (Group3), rising PSA after local therapy (Group4), and metastatic patients (Group5). Gal-3 and PSA level were divided by their respective autoantibodies, which yielded relative PSA and relative Gal-3 levels. After the adjustments, Spearman's rank correlations and linear regression modeling revealed the positive associations between relative Gal-3 and relative PSA levels among all 95 men combined (rho = 0.446, P < 0.0001; fitted slope 0.448, P < 0.0001), in Group2 (rho = 0.616, P = 0.0050; fitted slope 0.438, P =0.0011), and Group3 (rho = 0.484, P = 0.0360; fitted slope 0.470, P = 0.0187). The data show positive associations of relative Gal-3 and relative PSA levels in prostate cancer patients, notably at early clinical time course. Allowing for the influence of autoantibodies, Gal-3 level might be considered as a potential biomarker since it is positively associated with PSA level.
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spelling pubmed-53476902017-03-31 Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I Nakajima, Kosei Heilbrun, Lance K Hogan, Victor Smith, Daryn Heath, Elisabeth Raz, Avraham Oncotarget Research Paper Galectin-3 (Gal-3), an oncogenic pro-inflammatory protein, has been suggested as a possible complementary diagnostic candidate to prostate specific antigen (PSA) blood test for prostate cancer patients. The presence of the proteins in the circulation (biomarkers) may elicit an intrinsic humoral immune reaction by generating autoantibodies, which consequently could alter the detection levels. Here, we report the associations of the two prostate cancer biomarkers, Gal-3 and PSA in patients at different clinical states of prostate cancer while taking into account the autoantibody levels. A blind, prospective, single institution, pilot study was conducted. A total of 95 men were classified into 5 groups: healthy controls (Group1), newly diagnosed patients (Group2), no recurrence after local therapy (Group3), rising PSA after local therapy (Group4), and metastatic patients (Group5). Gal-3 and PSA level were divided by their respective autoantibodies, which yielded relative PSA and relative Gal-3 levels. After the adjustments, Spearman's rank correlations and linear regression modeling revealed the positive associations between relative Gal-3 and relative PSA levels among all 95 men combined (rho = 0.446, P < 0.0001; fitted slope 0.448, P < 0.0001), in Group2 (rho = 0.616, P = 0.0050; fitted slope 0.438, P =0.0011), and Group3 (rho = 0.484, P = 0.0360; fitted slope 0.470, P = 0.0187). The data show positive associations of relative Gal-3 and relative PSA levels in prostate cancer patients, notably at early clinical time course. Allowing for the influence of autoantibodies, Gal-3 level might be considered as a potential biomarker since it is positively associated with PSA level. Impact Journals LLC 2016-10-12 /pmc/articles/PMC5347690/ /pubmed/27741512 http://dx.doi.org/10.18632/oncotarget.12619 Text en Copyright: © 2016 Nakajima et al. http://creativecommons.org/licenses/by/3.0/ 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
Nakajima, Kosei
Heilbrun, Lance K
Hogan, Victor
Smith, Daryn
Heath, Elisabeth
Raz, Avraham
Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title_full Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title_fullStr Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title_full_unstemmed Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title_short Positive associations between galectin-3 and PSA levels in prostate cancer patients: a prospective clinical study-I
title_sort positive associations between galectin-3 and psa levels in prostate cancer patients: a prospective clinical study-i
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347690/
https://www.ncbi.nlm.nih.gov/pubmed/27741512
http://dx.doi.org/10.18632/oncotarget.12619
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