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Genomic and proteomic biomarker landscape in clinical trials

The use of molecular biomarkers to support disease diagnosis, monitor its progression, and guide drug treatment has gained traction in the last decades. While only a dozen biomarkers have been approved for their exploitation in the clinic by the FDA, many more are evaluated in the context of transla...

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Autores principales: Piñero, Janet, Rodriguez Fraga, Pablo S., Valls-Margarit, Jordi, Ronzano, Francesco, Accuosto, Pablo, Lambea Jane, Ricard, Sanz, Ferran, Furlong, Laura I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036891/
https://www.ncbi.nlm.nih.gov/pubmed/36968019
http://dx.doi.org/10.1016/j.csbj.2023.03.014
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author Piñero, Janet
Rodriguez Fraga, Pablo S.
Valls-Margarit, Jordi
Ronzano, Francesco
Accuosto, Pablo
Lambea Jane, Ricard
Sanz, Ferran
Furlong, Laura I.
author_facet Piñero, Janet
Rodriguez Fraga, Pablo S.
Valls-Margarit, Jordi
Ronzano, Francesco
Accuosto, Pablo
Lambea Jane, Ricard
Sanz, Ferran
Furlong, Laura I.
author_sort Piñero, Janet
collection PubMed
description The use of molecular biomarkers to support disease diagnosis, monitor its progression, and guide drug treatment has gained traction in the last decades. While only a dozen biomarkers have been approved for their exploitation in the clinic by the FDA, many more are evaluated in the context of translational research and clinical trials. Furthermore, the information on which biomarkers are measured, for which purpose, and in relation to which conditions are not readily accessible: biomarkers used in clinical studies available through resources such as ClinicalTrials.gov are described as free text, posing significant challenges in finding, analyzing, and processing them by both humans and machines. We present a text mining strategy to identify proteomic and genomic biomarkers used in clinical trials and classify them according to the methodologies by which they are measured. We find more than 3000 biomarkers used in the context of 2600 diseases. By analyzing this dataset, we uncover patterns of use of biomarkers across therapeutic areas over time, including the biomarker type and their specificity. These data are made available at the Clinical Biomarker App at https://www.disgenet.org/biomarkers/, a new portal that enables the exploration of biomarkers extracted from the clinical studies available at ClinicalTrials.gov and enriched with information from the scientific literature. The App features several metrics that assess the specificity of the biomarkers, facilitating their selection and prioritization. Overall, the Clinical Biomarker App is a valuable and timely resource about clinical biomarkers, to accelerate biomarker discovery, development, and application.
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spelling pubmed-100368912023-03-25 Genomic and proteomic biomarker landscape in clinical trials Piñero, Janet Rodriguez Fraga, Pablo S. Valls-Margarit, Jordi Ronzano, Francesco Accuosto, Pablo Lambea Jane, Ricard Sanz, Ferran Furlong, Laura I. Comput Struct Biotechnol J Research Article The use of molecular biomarkers to support disease diagnosis, monitor its progression, and guide drug treatment has gained traction in the last decades. While only a dozen biomarkers have been approved for their exploitation in the clinic by the FDA, many more are evaluated in the context of translational research and clinical trials. Furthermore, the information on which biomarkers are measured, for which purpose, and in relation to which conditions are not readily accessible: biomarkers used in clinical studies available through resources such as ClinicalTrials.gov are described as free text, posing significant challenges in finding, analyzing, and processing them by both humans and machines. We present a text mining strategy to identify proteomic and genomic biomarkers used in clinical trials and classify them according to the methodologies by which they are measured. We find more than 3000 biomarkers used in the context of 2600 diseases. By analyzing this dataset, we uncover patterns of use of biomarkers across therapeutic areas over time, including the biomarker type and their specificity. These data are made available at the Clinical Biomarker App at https://www.disgenet.org/biomarkers/, a new portal that enables the exploration of biomarkers extracted from the clinical studies available at ClinicalTrials.gov and enriched with information from the scientific literature. The App features several metrics that assess the specificity of the biomarkers, facilitating their selection and prioritization. Overall, the Clinical Biomarker App is a valuable and timely resource about clinical biomarkers, to accelerate biomarker discovery, development, and application. Research Network of Computational and Structural Biotechnology 2023-03-16 /pmc/articles/PMC10036891/ /pubmed/36968019 http://dx.doi.org/10.1016/j.csbj.2023.03.014 Text en © 2023 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Piñero, Janet
Rodriguez Fraga, Pablo S.
Valls-Margarit, Jordi
Ronzano, Francesco
Accuosto, Pablo
Lambea Jane, Ricard
Sanz, Ferran
Furlong, Laura I.
Genomic and proteomic biomarker landscape in clinical trials
title Genomic and proteomic biomarker landscape in clinical trials
title_full Genomic and proteomic biomarker landscape in clinical trials
title_fullStr Genomic and proteomic biomarker landscape in clinical trials
title_full_unstemmed Genomic and proteomic biomarker landscape in clinical trials
title_short Genomic and proteomic biomarker landscape in clinical trials
title_sort genomic and proteomic biomarker landscape in clinical trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036891/
https://www.ncbi.nlm.nih.gov/pubmed/36968019
http://dx.doi.org/10.1016/j.csbj.2023.03.014
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