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Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy
Liquid biopsy, based on the circulating tumor cells (CTCs) and cell-free nucleic acids has potential applications at multiple points throughout the natural course of cancer, from diagnosis to follow-up. The advantages of doing ctDNA assessment vs. tissue-based genomic profile are the minimal procedu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407029/ https://www.ncbi.nlm.nih.gov/pubmed/30736478 http://dx.doi.org/10.3390/cancers11020196 |
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author | Cimadamore, Alessia Gasparrini, Silvia Massari, Francesco Santoni, Matteo Cheng, Liang Lopez-Beltran, Antonio Scarpelli, Marina Montironi, Rodolfo |
author_facet | Cimadamore, Alessia Gasparrini, Silvia Massari, Francesco Santoni, Matteo Cheng, Liang Lopez-Beltran, Antonio Scarpelli, Marina Montironi, Rodolfo |
author_sort | Cimadamore, Alessia |
collection | PubMed |
description | Liquid biopsy, based on the circulating tumor cells (CTCs) and cell-free nucleic acids has potential applications at multiple points throughout the natural course of cancer, from diagnosis to follow-up. The advantages of doing ctDNA assessment vs. tissue-based genomic profile are the minimal procedural risk, the possibility to serial testing in order to monitor disease-relapse and response to therapy over time and to reduce hospitalization costs during the entire process. However, some critical issues related to ctDNA assays should be taken into consideration. The sensitivity of ctDNA assays depends on the assessment technique and genetic platforms used, on tumor-organ, stage, tumor heterogeneity, tumor clonality. The specificity is usually very high, whereas the concordance with tumor-based biopsy is generally low. In patients with renal cell carcinoma (RCC), qualitative analyses of ctDNA have been performed with interesting results regarding selective pressure from therapy, therapeutic resistance, exceptional treatment response to everolimus and mutations associated with aggressive behavior. Quantitative analyses showed variations of ccfDNA levels at different tumor stage. Compared to CTC assay, ctDNA is more stable than cells and easier to isolate. Splice variants, information at single-cell level and functional assays along with proteomics, transcriptomics and metabolomics studies can be performed only in CTCs. |
format | Online Article Text |
id | pubmed-6407029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64070292019-03-21 Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy Cimadamore, Alessia Gasparrini, Silvia Massari, Francesco Santoni, Matteo Cheng, Liang Lopez-Beltran, Antonio Scarpelli, Marina Montironi, Rodolfo Cancers (Basel) Review Liquid biopsy, based on the circulating tumor cells (CTCs) and cell-free nucleic acids has potential applications at multiple points throughout the natural course of cancer, from diagnosis to follow-up. The advantages of doing ctDNA assessment vs. tissue-based genomic profile are the minimal procedural risk, the possibility to serial testing in order to monitor disease-relapse and response to therapy over time and to reduce hospitalization costs during the entire process. However, some critical issues related to ctDNA assays should be taken into consideration. The sensitivity of ctDNA assays depends on the assessment technique and genetic platforms used, on tumor-organ, stage, tumor heterogeneity, tumor clonality. The specificity is usually very high, whereas the concordance with tumor-based biopsy is generally low. In patients with renal cell carcinoma (RCC), qualitative analyses of ctDNA have been performed with interesting results regarding selective pressure from therapy, therapeutic resistance, exceptional treatment response to everolimus and mutations associated with aggressive behavior. Quantitative analyses showed variations of ccfDNA levels at different tumor stage. Compared to CTC assay, ctDNA is more stable than cells and easier to isolate. Splice variants, information at single-cell level and functional assays along with proteomics, transcriptomics and metabolomics studies can be performed only in CTCs. MDPI 2019-02-07 /pmc/articles/PMC6407029/ /pubmed/30736478 http://dx.doi.org/10.3390/cancers11020196 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Cimadamore, Alessia Gasparrini, Silvia Massari, Francesco Santoni, Matteo Cheng, Liang Lopez-Beltran, Antonio Scarpelli, Marina Montironi, Rodolfo Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title | Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title_full | Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title_fullStr | Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title_full_unstemmed | Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title_short | Emerging Molecular Technologies in Renal Cell Carcinoma: Liquid Biopsy |
title_sort | emerging molecular technologies in renal cell carcinoma: liquid biopsy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407029/ https://www.ncbi.nlm.nih.gov/pubmed/30736478 http://dx.doi.org/10.3390/cancers11020196 |
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