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Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer

Infectious agents, including the BK polyomavirus (BKPyV), have been proposed as important inflammatory pathogens in prostate cancer. Here, we evaluated whether the preoperative antibody response to BKPyV large T antigen (LTag) and viral capsid protein 1 (VP1) was associated with the risk of biochemi...

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Autores principales: Keller, Xavier Etienne, Kardas, Piotr, Acevedo, Claudio, Sais, Giovanni, Poyet, Cédric, Banzola, Irina, Mortezavi, Ashkan, Seifert, Burkhardt, Sulser, Tullio, Hirsch, Hans H., Provenzano, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467449/
https://www.ncbi.nlm.nih.gov/pubmed/25749042
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author Keller, Xavier Etienne
Kardas, Piotr
Acevedo, Claudio
Sais, Giovanni
Poyet, Cédric
Banzola, Irina
Mortezavi, Ashkan
Seifert, Burkhardt
Sulser, Tullio
Hirsch, Hans H.
Provenzano, Maurizio
author_facet Keller, Xavier Etienne
Kardas, Piotr
Acevedo, Claudio
Sais, Giovanni
Poyet, Cédric
Banzola, Irina
Mortezavi, Ashkan
Seifert, Burkhardt
Sulser, Tullio
Hirsch, Hans H.
Provenzano, Maurizio
author_sort Keller, Xavier Etienne
collection PubMed
description Infectious agents, including the BK polyomavirus (BKPyV), have been proposed as important inflammatory pathogens in prostate cancer. Here, we evaluated whether the preoperative antibody response to BKPyV large T antigen (LTag) and viral capsid protein 1 (VP1) was associated with the risk of biochemical recurrence in 226 patients undergoing radical prostatectomy for primary prostate cancer. Essentially, the multivariate Cox regression analysis revealed that preoperative seropositivity to BKPyV LTag significantly reduced the risk of biochemical recurrence, independently of established predictors of biochemical recurrence such as tumor stage, Gleason score and surgical margin status. The predictive accuracy of the regression model was denotatively increased by the inclusion of the BKPyV LTag serostatus. In contrast, the VP1 serostatus was of no prognostic value. Finally, the BKPyV LTag serostatus was associated with a peculiar cytokine gene expression profile upon assessment of the cellular immune response elicited by LTag. Taken together, our findings suggest that the BKPyV LTag serology may serve as a prognostic factor in prostate cancer. If validated in additional studies, this biomarker may allow for better treatment decisions after radical prostatectomy. Finally, the favorable outcome of LTag seropositive patients may provide a potential opportunity for novel therapeutic approaches targeting a viral antigen.
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spelling pubmed-44674492015-06-22 Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer Keller, Xavier Etienne Kardas, Piotr Acevedo, Claudio Sais, Giovanni Poyet, Cédric Banzola, Irina Mortezavi, Ashkan Seifert, Burkhardt Sulser, Tullio Hirsch, Hans H. Provenzano, Maurizio Oncotarget Clinical Research Paper Infectious agents, including the BK polyomavirus (BKPyV), have been proposed as important inflammatory pathogens in prostate cancer. Here, we evaluated whether the preoperative antibody response to BKPyV large T antigen (LTag) and viral capsid protein 1 (VP1) was associated with the risk of biochemical recurrence in 226 patients undergoing radical prostatectomy for primary prostate cancer. Essentially, the multivariate Cox regression analysis revealed that preoperative seropositivity to BKPyV LTag significantly reduced the risk of biochemical recurrence, independently of established predictors of biochemical recurrence such as tumor stage, Gleason score and surgical margin status. The predictive accuracy of the regression model was denotatively increased by the inclusion of the BKPyV LTag serostatus. In contrast, the VP1 serostatus was of no prognostic value. Finally, the BKPyV LTag serostatus was associated with a peculiar cytokine gene expression profile upon assessment of the cellular immune response elicited by LTag. Taken together, our findings suggest that the BKPyV LTag serology may serve as a prognostic factor in prostate cancer. If validated in additional studies, this biomarker may allow for better treatment decisions after radical prostatectomy. Finally, the favorable outcome of LTag seropositive patients may provide a potential opportunity for novel therapeutic approaches targeting a viral antigen. Impact Journals LLC 2015-01-31 /pmc/articles/PMC4467449/ /pubmed/25749042 Text en Copyright: © 2015 Keller 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 Clinical Research Paper
Keller, Xavier Etienne
Kardas, Piotr
Acevedo, Claudio
Sais, Giovanni
Poyet, Cédric
Banzola, Irina
Mortezavi, Ashkan
Seifert, Burkhardt
Sulser, Tullio
Hirsch, Hans H.
Provenzano, Maurizio
Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title_full Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title_fullStr Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title_full_unstemmed Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title_short Antibody response to BK polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
title_sort antibody response to bk polyomavirus as a prognostic biomarker and potential therapeutic target in prostate cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467449/
https://www.ncbi.nlm.nih.gov/pubmed/25749042
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