Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer

Detalhes bibliográficos
Autor(a) principal: Gardani, Carla Fernanda Furtado
Data de Publicação: 2023
Outros Autores: Pedrazza, Eduardo Luiz, Paz, Victória Santos, Zanirati, Gabriele Goulart, Costa, Jaderson Costa da, Andrejew, Roberta, Ulrich, Henning, Scholl, Juliete Nathali, Figueiró, Fabrício, Rockenbach, Liliana, Morrone, Fernanda Bueno
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/268368
Resumo: Prostate cancer (PC) is the most diagnosed tumor in males and ranks as the second leading cause of male mortality in the western world. The CD39 and CD73 enzymes play a crucial role in cancer regulation by degrading nucleotides and forming nucleosides. This study aimed to investigate the expression of the CD39 and CD73 enzymes as potential therapeutic targets for PC. The initial part of this study retrospectively analyzed tissue samples from 23 PC patients. Using the TissueFAXSTM cytometry platform, we found significantly higher levels of CD39—labeling its intensity compared to CD73. Additionally, we observed a correlation between the Gleason score and the intensity of CD39 expression. In the prospective arm, blood samples were collected from 25 patients at the time of diagnosis and after six months of treatment to determine the expression of CD39 and CD73 in the serum extracellular vesicles (EVs) and to analyze nucleotide hydrolysis. Notably, the expression of CD39 in the EVs was significantly increased compared to the CD73 and/or combined CD39/CD73 expression levels at initial collection. Furthermore, our results demonstrated positive correlations between ADP hydrolysis and the transurethral resection and Gleason score. Understanding the role of ectonucleotidases is crucial for identifying new biomarkers in PC.
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spelling Gardani, Carla Fernanda FurtadoPedrazza, Eduardo LuizPaz, Victória SantosZanirati, Gabriele GoulartCosta, Jaderson Costa daAndrejew, RobertaUlrich, HenningScholl, Juliete NathaliFigueiró, FabrícioRockenbach, LilianaMorrone, Fernanda Bueno2023-12-13T03:26:13Z20231424-8247http://hdl.handle.net/10183/268368001189416Prostate cancer (PC) is the most diagnosed tumor in males and ranks as the second leading cause of male mortality in the western world. The CD39 and CD73 enzymes play a crucial role in cancer regulation by degrading nucleotides and forming nucleosides. This study aimed to investigate the expression of the CD39 and CD73 enzymes as potential therapeutic targets for PC. The initial part of this study retrospectively analyzed tissue samples from 23 PC patients. Using the TissueFAXSTM cytometry platform, we found significantly higher levels of CD39—labeling its intensity compared to CD73. Additionally, we observed a correlation between the Gleason score and the intensity of CD39 expression. In the prospective arm, blood samples were collected from 25 patients at the time of diagnosis and after six months of treatment to determine the expression of CD39 and CD73 in the serum extracellular vesicles (EVs) and to analyze nucleotide hydrolysis. Notably, the expression of CD39 in the EVs was significantly increased compared to the CD73 and/or combined CD39/CD73 expression levels at initial collection. Furthermore, our results demonstrated positive correlations between ADP hydrolysis and the transurethral resection and Gleason score. Understanding the role of ectonucleotidases is crucial for identifying new biomarkers in PC.application/pdfengPharmaceuticals. Basel. Vol. 16, no. 11 (Nov. 2023), 1619, 17 p.BiomarcadoresNeoplasias da próstataVesículas extracelularesProstate cancerEctonucleotidasesCD39CD73Extracellular vesiclesExploring CD39 and CD73 expression as potential biomarkers in prostate cancerEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001189416.pdf.txt001189416.pdf.txtExtracted Texttext/plain65730http://www.lume.ufrgs.br/bitstream/10183/268368/2/001189416.pdf.txteb1e7ef57d5f28b9d51794a9defe2aacMD52ORIGINAL001189416.pdfTexto completo (inglês)application/pdf1911218http://www.lume.ufrgs.br/bitstream/10183/268368/1/001189416.pdf7c3cbda0e9cbaf196eb25c3afb41bcd9MD5110183/2683682023-12-14 04:24:23.71882oai:www.lume.ufrgs.br:10183/268368Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-12-14T06:24:23Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
title Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
spellingShingle Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
Gardani, Carla Fernanda Furtado
Biomarcadores
Neoplasias da próstata
Vesículas extracelulares
Prostate cancer
Ectonucleotidases
CD39
CD73
Extracellular vesicles
title_short Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
title_full Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
title_fullStr Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
title_full_unstemmed Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
title_sort Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
author Gardani, Carla Fernanda Furtado
author_facet Gardani, Carla Fernanda Furtado
Pedrazza, Eduardo Luiz
Paz, Victória Santos
Zanirati, Gabriele Goulart
Costa, Jaderson Costa da
Andrejew, Roberta
Ulrich, Henning
Scholl, Juliete Nathali
Figueiró, Fabrício
Rockenbach, Liliana
Morrone, Fernanda Bueno
author_role author
author2 Pedrazza, Eduardo Luiz
Paz, Victória Santos
Zanirati, Gabriele Goulart
Costa, Jaderson Costa da
Andrejew, Roberta
Ulrich, Henning
Scholl, Juliete Nathali
Figueiró, Fabrício
Rockenbach, Liliana
Morrone, Fernanda Bueno
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gardani, Carla Fernanda Furtado
Pedrazza, Eduardo Luiz
Paz, Victória Santos
Zanirati, Gabriele Goulart
Costa, Jaderson Costa da
Andrejew, Roberta
Ulrich, Henning
Scholl, Juliete Nathali
Figueiró, Fabrício
Rockenbach, Liliana
Morrone, Fernanda Bueno
dc.subject.por.fl_str_mv Biomarcadores
Neoplasias da próstata
Vesículas extracelulares
topic Biomarcadores
Neoplasias da próstata
Vesículas extracelulares
Prostate cancer
Ectonucleotidases
CD39
CD73
Extracellular vesicles
dc.subject.eng.fl_str_mv Prostate cancer
Ectonucleotidases
CD39
CD73
Extracellular vesicles
description Prostate cancer (PC) is the most diagnosed tumor in males and ranks as the second leading cause of male mortality in the western world. The CD39 and CD73 enzymes play a crucial role in cancer regulation by degrading nucleotides and forming nucleosides. This study aimed to investigate the expression of the CD39 and CD73 enzymes as potential therapeutic targets for PC. The initial part of this study retrospectively analyzed tissue samples from 23 PC patients. Using the TissueFAXSTM cytometry platform, we found significantly higher levels of CD39—labeling its intensity compared to CD73. Additionally, we observed a correlation between the Gleason score and the intensity of CD39 expression. In the prospective arm, blood samples were collected from 25 patients at the time of diagnosis and after six months of treatment to determine the expression of CD39 and CD73 in the serum extracellular vesicles (EVs) and to analyze nucleotide hydrolysis. Notably, the expression of CD39 in the EVs was significantly increased compared to the CD73 and/or combined CD39/CD73 expression levels at initial collection. Furthermore, our results demonstrated positive correlations between ADP hydrolysis and the transurethral resection and Gleason score. Understanding the role of ectonucleotidases is crucial for identifying new biomarkers in PC.
publishDate 2023
dc.date.accessioned.fl_str_mv 2023-12-13T03:26:13Z
dc.date.issued.fl_str_mv 2023
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dc.identifier.nrb.pt_BR.fl_str_mv 001189416
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Pharmaceuticals. Basel. Vol. 16, no. 11 (Nov. 2023), 1619, 17 p.
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