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Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets

Over the past few decades, drug discovery has greatly improved the outcomes for patients, but several challenges continue to hinder the rapid development of novel drugs. Addressing unmet clinical needs requires the pursuit of drug targets that have a higher likelihood to lead to the development of s...

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Detalles Bibliográficos
Autores principales: Beis, G., Serafeim, A.P., Papasotiriou, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732000/
https://www.ncbi.nlm.nih.gov/pubmed/36514341
http://dx.doi.org/10.1016/j.csbj.2022.11.042
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author Beis, G.
Serafeim, A.P.
Papasotiriou, I.
author_facet Beis, G.
Serafeim, A.P.
Papasotiriou, I.
author_sort Beis, G.
collection PubMed
description Over the past few decades, drug discovery has greatly improved the outcomes for patients, but several challenges continue to hinder the rapid development of novel drugs. Addressing unmet clinical needs requires the pursuit of drug targets that have a higher likelihood to lead to the development of successful drugs. Here we describe a bioinformatic approach for identifying novel cancer drug targets by performing statistical analysis to ascertain quantitative changes in expression levels between protein-coding genes, as well as co-expression networks to classify these genes into groups. Subsequently, we provide an overview of druggability assessment methodologies to prioritize and select the best targets to pursue.
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spelling pubmed-97320002022-12-12 Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets Beis, G. Serafeim, A.P. Papasotiriou, I. Comput Struct Biotechnol J Review Over the past few decades, drug discovery has greatly improved the outcomes for patients, but several challenges continue to hinder the rapid development of novel drugs. Addressing unmet clinical needs requires the pursuit of drug targets that have a higher likelihood to lead to the development of successful drugs. Here we describe a bioinformatic approach for identifying novel cancer drug targets by performing statistical analysis to ascertain quantitative changes in expression levels between protein-coding genes, as well as co-expression networks to classify these genes into groups. Subsequently, we provide an overview of druggability assessment methodologies to prioritize and select the best targets to pursue. Research Network of Computational and Structural Biotechnology 2022-11-24 /pmc/articles/PMC9732000/ /pubmed/36514341 http://dx.doi.org/10.1016/j.csbj.2022.11.042 Text en © 2022 RGCC International GmbH 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 Review
Beis, G.
Serafeim, A.P.
Papasotiriou, I.
Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title_full Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title_fullStr Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title_full_unstemmed Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title_short Data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
title_sort data-driven analysis and druggability assessment methods to accelerate the identification of novel cancer targets
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732000/
https://www.ncbi.nlm.nih.gov/pubmed/36514341
http://dx.doi.org/10.1016/j.csbj.2022.11.042
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