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dc.contributor.authorChadha, M
dc.contributor.authorHuang, PH
dc.coverage.spatialUnited States
dc.date.accessioned2022-09-06T11:43:13Z
dc.date.available2022-09-06T11:43:13Z
dc.date.issued2022-02-16
dc.identifier10.1007/s11864-022-00947-3
dc.identifier.citationCurrent Treatment Options in Oncology, 2022, 23 (1), pp. 78 - 88
dc.identifier.issn1527-2729
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5418
dc.identifier.eissn1534-6277
dc.identifier.eissn1534-6277
dc.identifier.doi10.1007/s11864-022-00947-3
dc.description.abstractAdvances in proteomic and metabolomic technologies have accelerated our understanding of multiple aspects of cancer biology across distinct tumour types. Here we review the current state-of-the-art in the use of proteomics and metabolomics in soft tissue sarcomas. We highlight the utility of these Omics-based methodologies to identify new drug targets, synthetic lethal interactions, candidate therapeutics and novel biomarkers to facilitate patient stratification. Due to the unbiased and global nature of these profiling methods to assess the levels of protein expression, post-translational modifications such as phosphorylation and glycosylation as well as key metabolites, many of these findings have broad applications not just in specific histotypes but across multiple STS subtypes. Specific examples of proteomic and metabolomic findings that have led to the development of early phase clinical trials of investigational agents will be discussed. While promising, the use of these technologies in the study of sarcoma is still limited, and there is a need for further research in this area. In particular, it would be important to integrate these approaches with other Omics strategies such as genomics and epigenomics as well as implement these tools alongside clinical trials in order to maximize the impact of these tools on our biological understanding and treatment of this group of rare diseases of unmet need.
dc.formatPrint-Electronic
dc.format.extent78 - 88
dc.languageeng
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.ispartofCurrent Treatment Options in Oncology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBiomarkers
dc.subjectDrug discovery
dc.subjectMetabolomics
dc.subjectProteomics
dc.subjectSarcoma
dc.subjectEpigenomics
dc.subjectGenomics
dc.subjectHumans
dc.subjectMetabolomics
dc.subjectProteomics
dc.subjectSarcoma
dc.subjectSoft Tissue Neoplasms
dc.titleProteomic and Metabolomic Profiling in Soft Tissue Sarcomas.
dc.typeJournal Article
dcterms.dateAccepted2021-12-04
dc.date.updated2022-09-06T11:42:43Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1007/s11864-022-00947-3
rioxxterms.licenseref.startdate2022-02-16
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35171456
pubs.issue1
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Molecular and Systems Oncology
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1007/s11864-022-00947-3
pubs.volume23
icr.researchteamMol and Systems Oncology
dc.contributor.icrauthorChadha, Madhumeeta
dc.contributor.icrauthorHuang, Paul
icr.provenanceDeposited by Mr Arek Surman on 2022-09-06. Deposit type is initial. No. of files: 1. Files: Proteomic and Metabolomic Profiling in Soft Tissue Sarcomas.pdf


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