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Urinary Markers in Bladder Cancer: An Update
Bladder cancer (BC) is ones of the most common cancer worldwide. It is classified in muscle invasive (MIBC) and muscle non-invasive (NMIBC) BC. NMIBCs frequently recur and progress to MIBCs with a reduced survival rate and frequent distant metastasis. BC detection require unpleasant and expensive cy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137202/ https://www.ncbi.nlm.nih.gov/pubmed/30245975 http://dx.doi.org/10.3389/fonc.2018.00362 |
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author | Santoni, Giorgio Morelli, Maria B. Amantini, Consuelo Battelli, Nicola |
author_facet | Santoni, Giorgio Morelli, Maria B. Amantini, Consuelo Battelli, Nicola |
author_sort | Santoni, Giorgio |
collection | PubMed |
description | Bladder cancer (BC) is ones of the most common cancer worldwide. It is classified in muscle invasive (MIBC) and muscle non-invasive (NMIBC) BC. NMIBCs frequently recur and progress to MIBCs with a reduced survival rate and frequent distant metastasis. BC detection require unpleasant and expensive cystoscopy and biopsy, which are often accompanied by several adverse effects. Thus, there is an urgent need to develop novel diagnostic methods for initial detection and surveillance in both MIBCs and NMIBCs. Multiple urine-based tests approved by FDA for BC detection and surveillance are commercially available. However, at present, sensitivity, specificity and diagnostic accuracy of these urine-based assays are still suboptimal and, in the attend to improve them, novel molecular markers as well as multiple-assays must to be translated in clinic. Now there are growing evidence toward the use of minimally invasive “liquid biopsy” to identify biomarkers in urologic malignancy. DNA- and RNA-based markers in body fluids such as blood and urine are promising potential markers in diagnostic, prognostic, predictive and monitoring urological malignancies. Thus, circulating cell-free DNA, DNA methylation and mutations, circulating tumor cells, miRNA, IncRNA and mRNAs, cell-free proteins and peptides, and exosomes have been assessed in urine specimens. However, proteomic and genomic data must to be validated in well-designed multicenter clinical studies, before to be employed in clinic oncology. |
format | Online Article Text |
id | pubmed-6137202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61372022018-09-21 Urinary Markers in Bladder Cancer: An Update Santoni, Giorgio Morelli, Maria B. Amantini, Consuelo Battelli, Nicola Front Oncol Oncology Bladder cancer (BC) is ones of the most common cancer worldwide. It is classified in muscle invasive (MIBC) and muscle non-invasive (NMIBC) BC. NMIBCs frequently recur and progress to MIBCs with a reduced survival rate and frequent distant metastasis. BC detection require unpleasant and expensive cystoscopy and biopsy, which are often accompanied by several adverse effects. Thus, there is an urgent need to develop novel diagnostic methods for initial detection and surveillance in both MIBCs and NMIBCs. Multiple urine-based tests approved by FDA for BC detection and surveillance are commercially available. However, at present, sensitivity, specificity and diagnostic accuracy of these urine-based assays are still suboptimal and, in the attend to improve them, novel molecular markers as well as multiple-assays must to be translated in clinic. Now there are growing evidence toward the use of minimally invasive “liquid biopsy” to identify biomarkers in urologic malignancy. DNA- and RNA-based markers in body fluids such as blood and urine are promising potential markers in diagnostic, prognostic, predictive and monitoring urological malignancies. Thus, circulating cell-free DNA, DNA methylation and mutations, circulating tumor cells, miRNA, IncRNA and mRNAs, cell-free proteins and peptides, and exosomes have been assessed in urine specimens. However, proteomic and genomic data must to be validated in well-designed multicenter clinical studies, before to be employed in clinic oncology. Frontiers Media S.A. 2018-09-07 /pmc/articles/PMC6137202/ /pubmed/30245975 http://dx.doi.org/10.3389/fonc.2018.00362 Text en Copyright © 2018 Santoni, Morelli, Amantini and Battelli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Santoni, Giorgio Morelli, Maria B. Amantini, Consuelo Battelli, Nicola Urinary Markers in Bladder Cancer: An Update |
title | Urinary Markers in Bladder Cancer: An Update |
title_full | Urinary Markers in Bladder Cancer: An Update |
title_fullStr | Urinary Markers in Bladder Cancer: An Update |
title_full_unstemmed | Urinary Markers in Bladder Cancer: An Update |
title_short | Urinary Markers in Bladder Cancer: An Update |
title_sort | urinary markers in bladder cancer: an update |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137202/ https://www.ncbi.nlm.nih.gov/pubmed/30245975 http://dx.doi.org/10.3389/fonc.2018.00362 |
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