Applications of transcriptomics in support of drug development for osteoarthritis

Objective: Understanding the heterogeneity and pathophysiology of osteoarthritis (OA) is critical to support the development of tailored disease-modifying treatments. To this aim, transcriptomics tools are highly relevant to delineate dysregulated molecular pathways and identify new therapeutic targ...

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Autores principales: Hélène Kaplon, Luo Yufei, Frédéric De Ceuninck, Agnès Lalande, Sophie Courtade-Gaiani, Laurence Laigle, Philippe Moingeon
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/4cf2075a13b540a8a40b0a21dab2775b
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spelling oai:doaj.org-article:4cf2075a13b540a8a40b0a21dab2775b2021-11-22T04:30:41ZApplications of transcriptomics in support of drug development for osteoarthritis2665-913110.1016/j.ocarto.2021.100221https://doaj.org/article/4cf2075a13b540a8a40b0a21dab2775b2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2665913121000844https://doaj.org/toc/2665-9131Objective: Understanding the heterogeneity and pathophysiology of osteoarthritis (OA) is critical to support the development of tailored disease-modifying treatments. To this aim, transcriptomics tools are highly relevant to delineate dysregulated molecular pathways and identify new therapeutic targets. Methods: We review the methodology and outcomes of transcriptomics studies conducted in OA, based on a comprehensive literature search of the PubMed and Google Scholar databases using the terms “osteoarthritis”, “OA”, “knee OA”, “hip OA”, “genes”, “RNA-seq”, “microarray”, “transcriptomic” and “PCR” as key words. Beyond target-focused RT-qPCR, more comprehensive techniques include microarrays, RNA sequencing (RNA-seq) and single cell RNA-seq analyses. Results: The standardization of those methods to ensure the quality of both RNA extraction and sequencing is critical to get meaningful insights. Transcriptomics studies have been conducted in various tissues involved in the pathogenesis of OA, including articular cartilage, subchondral bone and synovium, as well as in the blood of patients. Molecular pathways dysregulated in OA relate to cartilage degradation, matrix and bone remodeling, neurogenic pain, inflammation, apoptosis and angiogenesis. This knowledge has direct application to patient stratification and further, to the identification of candidate therapeutic targets and biomarkers intended to monitor OA progression. Conclusion: In light of its high-throughput capabilities and ability to provide comprehensive information on major biological processes, transcriptomics represents a powerful method to support the development of new disease-modifying drugs in OA.Hélène KaplonLuo YufeiFrédéric De CeuninckAgnès LalandeSophie Courtade-GaianiLaurence LaiglePhilippe MoingeonElsevierarticleDMOADsMolecular profilingOsteoarthritisTranscriptomicsDiseases of the musculoskeletal systemRC925-935ENOsteoarthritis and Cartilage Open, Vol 3, Iss 4, Pp 100221- (2021)
institution DOAJ
collection DOAJ
language EN
topic DMOADs
Molecular profiling
Osteoarthritis
Transcriptomics
Diseases of the musculoskeletal system
RC925-935
spellingShingle DMOADs
Molecular profiling
Osteoarthritis
Transcriptomics
Diseases of the musculoskeletal system
RC925-935
Hélène Kaplon
Luo Yufei
Frédéric De Ceuninck
Agnès Lalande
Sophie Courtade-Gaiani
Laurence Laigle
Philippe Moingeon
Applications of transcriptomics in support of drug development for osteoarthritis
description Objective: Understanding the heterogeneity and pathophysiology of osteoarthritis (OA) is critical to support the development of tailored disease-modifying treatments. To this aim, transcriptomics tools are highly relevant to delineate dysregulated molecular pathways and identify new therapeutic targets. Methods: We review the methodology and outcomes of transcriptomics studies conducted in OA, based on a comprehensive literature search of the PubMed and Google Scholar databases using the terms “osteoarthritis”, “OA”, “knee OA”, “hip OA”, “genes”, “RNA-seq”, “microarray”, “transcriptomic” and “PCR” as key words. Beyond target-focused RT-qPCR, more comprehensive techniques include microarrays, RNA sequencing (RNA-seq) and single cell RNA-seq analyses. Results: The standardization of those methods to ensure the quality of both RNA extraction and sequencing is critical to get meaningful insights. Transcriptomics studies have been conducted in various tissues involved in the pathogenesis of OA, including articular cartilage, subchondral bone and synovium, as well as in the blood of patients. Molecular pathways dysregulated in OA relate to cartilage degradation, matrix and bone remodeling, neurogenic pain, inflammation, apoptosis and angiogenesis. This knowledge has direct application to patient stratification and further, to the identification of candidate therapeutic targets and biomarkers intended to monitor OA progression. Conclusion: In light of its high-throughput capabilities and ability to provide comprehensive information on major biological processes, transcriptomics represents a powerful method to support the development of new disease-modifying drugs in OA.
format article
author Hélène Kaplon
Luo Yufei
Frédéric De Ceuninck
Agnès Lalande
Sophie Courtade-Gaiani
Laurence Laigle
Philippe Moingeon
author_facet Hélène Kaplon
Luo Yufei
Frédéric De Ceuninck
Agnès Lalande
Sophie Courtade-Gaiani
Laurence Laigle
Philippe Moingeon
author_sort Hélène Kaplon
title Applications of transcriptomics in support of drug development for osteoarthritis
title_short Applications of transcriptomics in support of drug development for osteoarthritis
title_full Applications of transcriptomics in support of drug development for osteoarthritis
title_fullStr Applications of transcriptomics in support of drug development for osteoarthritis
title_full_unstemmed Applications of transcriptomics in support of drug development for osteoarthritis
title_sort applications of transcriptomics in support of drug development for osteoarthritis
publisher Elsevier
publishDate 2021
url https://doaj.org/article/4cf2075a13b540a8a40b0a21dab2775b
work_keys_str_mv AT helenekaplon applicationsoftranscriptomicsinsupportofdrugdevelopmentforosteoarthritis
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AT agneslalande applicationsoftranscriptomicsinsupportofdrugdevelopmentforosteoarthritis
AT sophiecourtadegaiani applicationsoftranscriptomicsinsupportofdrugdevelopmentforosteoarthritis
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