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Molecular Signatures in Urologic Tumors

Urologic tumors continue to represent a huge fraction of cancer cases in the United States, with over 376,310 estimated new diagnoses in 2013. As with many types of tumors, urologic tumors vary greatly in their phenotype, ranging from minimally invasive to malignancies possessing great metastatic po...

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Detalles Bibliográficos
Autores principales: Larkin, Spencer, Kyprianou, Natasha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794787/
https://www.ncbi.nlm.nih.gov/pubmed/24018887
http://dx.doi.org/10.3390/ijms140918421
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author Larkin, Spencer
Kyprianou, Natasha
author_facet Larkin, Spencer
Kyprianou, Natasha
author_sort Larkin, Spencer
collection PubMed
description Urologic tumors continue to represent a huge fraction of cancer cases in the United States, with over 376,310 estimated new diagnoses in 2013. As with many types of tumors, urologic tumors vary greatly in their phenotype, ranging from minimally invasive to malignancies possessing great metastatic potential. The increasing need for more efficient and less invasive methods of cancer detection, as well as the ability to predict severity of the disease phenotype is readily evident—yet reliable methods remain elusive in a clinical setting today. Comprehensive panels of gene clusters are being developed toward the generation of molecular signatures in order to better diagnose urologic malignancies, and identify effective treatment strategies in the emerging era of personalized medicine. In this review, we discuss the current literature on the credibility and biomarker value of such molecular signatures in the context of clinical significance relating to the pathological aggressiveness of urologic tumors (prostate, bladder and renal cancer)—also exploiting their predictive potential in the response to treatment.
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spelling pubmed-37947872013-10-21 Molecular Signatures in Urologic Tumors Larkin, Spencer Kyprianou, Natasha Int J Mol Sci Review Urologic tumors continue to represent a huge fraction of cancer cases in the United States, with over 376,310 estimated new diagnoses in 2013. As with many types of tumors, urologic tumors vary greatly in their phenotype, ranging from minimally invasive to malignancies possessing great metastatic potential. The increasing need for more efficient and less invasive methods of cancer detection, as well as the ability to predict severity of the disease phenotype is readily evident—yet reliable methods remain elusive in a clinical setting today. Comprehensive panels of gene clusters are being developed toward the generation of molecular signatures in order to better diagnose urologic malignancies, and identify effective treatment strategies in the emerging era of personalized medicine. In this review, we discuss the current literature on the credibility and biomarker value of such molecular signatures in the context of clinical significance relating to the pathological aggressiveness of urologic tumors (prostate, bladder and renal cancer)—also exploiting their predictive potential in the response to treatment. MDPI 2013-09-06 /pmc/articles/PMC3794787/ /pubmed/24018887 http://dx.doi.org/10.3390/ijms140918421 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Larkin, Spencer
Kyprianou, Natasha
Molecular Signatures in Urologic Tumors
title Molecular Signatures in Urologic Tumors
title_full Molecular Signatures in Urologic Tumors
title_fullStr Molecular Signatures in Urologic Tumors
title_full_unstemmed Molecular Signatures in Urologic Tumors
title_short Molecular Signatures in Urologic Tumors
title_sort molecular signatures in urologic tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794787/
https://www.ncbi.nlm.nih.gov/pubmed/24018887
http://dx.doi.org/10.3390/ijms140918421
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