Exploring CD39 and CD73 expression as potential biomarkers in prostate cancer
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , , |
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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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 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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article |
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http://hdl.handle.net/10183/268368 |
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1424-8247 |
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001189416 |
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http://hdl.handle.net/10183/268368 |
dc.language.iso.fl_str_mv |
eng |
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eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Pharmaceuticals. Basel. Vol. 16, no. 11 (Nov. 2023), 1619, 17 p. |
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info:eu-repo/semantics/openAccess |
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openAccess |
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