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Selecting the right therapeutic target for kidney disease
Kidney disease is a complex disease with several different etiologies and underlying associated pathophysiology. This is reflected by the lack of effective treatment therapies in chronic kidney disease (CKD) that stop disease progression. However, novel strategies, recent scientific breakthroughs, a...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666364/ https://www.ncbi.nlm.nih.gov/pubmed/36408217 http://dx.doi.org/10.3389/fphar.2022.971065 |
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author | Buvall, Lisa Menzies, Robert I. Williams, Julie Woollard, Kevin J. Kumar, Chanchal Granqvist, Anna B. Fritsch, Maria Feliers, Denis Reznichenko, Anna Gianni, Davide Petrovski, Slavé Bendtsen, Claus Bohlooly-Y, Mohammad Haefliger, Carolina Danielson, Regina Fritsche Hansen, Pernille B. L. |
author_facet | Buvall, Lisa Menzies, Robert I. Williams, Julie Woollard, Kevin J. Kumar, Chanchal Granqvist, Anna B. Fritsch, Maria Feliers, Denis Reznichenko, Anna Gianni, Davide Petrovski, Slavé Bendtsen, Claus Bohlooly-Y, Mohammad Haefliger, Carolina Danielson, Regina Fritsche Hansen, Pernille B. L. |
author_sort | Buvall, Lisa |
collection | PubMed |
description | Kidney disease is a complex disease with several different etiologies and underlying associated pathophysiology. This is reflected by the lack of effective treatment therapies in chronic kidney disease (CKD) that stop disease progression. However, novel strategies, recent scientific breakthroughs, and technological advances have revealed new possibilities for finding novel disease drivers in CKD. This review describes some of the latest advances in the field and brings them together in a more holistic framework as applied to identification and validation of disease drivers in CKD. It uses high-resolution ‘patient-centric’ omics data sets, advanced in silico tools (systems biology, connectivity mapping, and machine learning) and ‘state-of-the-art‘ experimental systems (complex 3D systems in vitro, CRISPR gene editing, and various model biological systems in vivo). Application of such a framework is expected to increase the likelihood of successful identification of novel drug candidates based on strong human target validation and a better scientific understanding of underlying mechanisms. |
format | Online Article Text |
id | pubmed-9666364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96663642022-11-17 Selecting the right therapeutic target for kidney disease Buvall, Lisa Menzies, Robert I. Williams, Julie Woollard, Kevin J. Kumar, Chanchal Granqvist, Anna B. Fritsch, Maria Feliers, Denis Reznichenko, Anna Gianni, Davide Petrovski, Slavé Bendtsen, Claus Bohlooly-Y, Mohammad Haefliger, Carolina Danielson, Regina Fritsche Hansen, Pernille B. L. Front Pharmacol Pharmacology Kidney disease is a complex disease with several different etiologies and underlying associated pathophysiology. This is reflected by the lack of effective treatment therapies in chronic kidney disease (CKD) that stop disease progression. However, novel strategies, recent scientific breakthroughs, and technological advances have revealed new possibilities for finding novel disease drivers in CKD. This review describes some of the latest advances in the field and brings them together in a more holistic framework as applied to identification and validation of disease drivers in CKD. It uses high-resolution ‘patient-centric’ omics data sets, advanced in silico tools (systems biology, connectivity mapping, and machine learning) and ‘state-of-the-art‘ experimental systems (complex 3D systems in vitro, CRISPR gene editing, and various model biological systems in vivo). Application of such a framework is expected to increase the likelihood of successful identification of novel drug candidates based on strong human target validation and a better scientific understanding of underlying mechanisms. Frontiers Media S.A. 2022-11-02 /pmc/articles/PMC9666364/ /pubmed/36408217 http://dx.doi.org/10.3389/fphar.2022.971065 Text en Copyright © 2022 Buvall, Menzies, Williams, Woollard, Kumar, Granqvist, Fritsch, Feliers, Reznichenko, Gianni, Petrovski, Bendtsen, Bohlooly-Y, Haefliger, Danielson and Hansen. https://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 | Pharmacology Buvall, Lisa Menzies, Robert I. Williams, Julie Woollard, Kevin J. Kumar, Chanchal Granqvist, Anna B. Fritsch, Maria Feliers, Denis Reznichenko, Anna Gianni, Davide Petrovski, Slavé Bendtsen, Claus Bohlooly-Y, Mohammad Haefliger, Carolina Danielson, Regina Fritsche Hansen, Pernille B. L. Selecting the right therapeutic target for kidney disease |
title | Selecting the right therapeutic target for kidney disease |
title_full | Selecting the right therapeutic target for kidney disease |
title_fullStr | Selecting the right therapeutic target for kidney disease |
title_full_unstemmed | Selecting the right therapeutic target for kidney disease |
title_short | Selecting the right therapeutic target for kidney disease |
title_sort | selecting the right therapeutic target for kidney disease |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666364/ https://www.ncbi.nlm.nih.gov/pubmed/36408217 http://dx.doi.org/10.3389/fphar.2022.971065 |
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