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dc.contributor.authorBurns, J
dc.contributor.authorWilding, CP
dc.contributor.authorKrasny, L
dc.contributor.authorZhu, X
dc.contributor.authorChadha, M
dc.contributor.authorTam, YB
dc.contributor.authorPs, H
dc.contributor.authorMahalingam, AH
dc.contributor.authorLee, ATJ
dc.contributor.authorArthur, A
dc.contributor.authorGuljar, N
dc.contributor.authorPerkins, E
dc.contributor.authorPankova, V
dc.contributor.authorJenks, A
dc.contributor.authorDjabatey, V
dc.contributor.authorSzecsei, C
dc.contributor.authorMcCarthy, F
dc.contributor.authorRagulan, C
dc.contributor.authorMilighetti, M
dc.contributor.authorRoumeliotis, TI
dc.contributor.authorCrosier, S
dc.contributor.authorFinetti, M
dc.contributor.authorChoudhary, JS
dc.contributor.authorJudson, I
dc.contributor.authorFisher, C
dc.contributor.authorSchuster, EF
dc.contributor.authorSadanandam, A
dc.contributor.authorChen, TW
dc.contributor.authorWilliamson, D
dc.contributor.authorThway, K
dc.contributor.authorJones, RL
dc.contributor.authorCheang, MCU
dc.contributor.authorHuang, PH
dc.coverage.spatialEngland
dc.date.accessioned2023-07-12T09:04:31Z
dc.date.available2023-07-12T09:04:31Z
dc.date.issued2023-06-29
dc.identifier3834
dc.identifier10.1038/s41467-023-39486-2
dc.identifier.citationNature Communications, 2023, 14 (1), pp. 3834 -
dc.identifier.issn2041-1723
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5885
dc.identifier.eissn2041-1723
dc.identifier.eissn2041-1723
dc.identifier.doi10.1038/s41467-023-39486-2
dc.description.abstractSoft tissue sarcomas (STS) are rare and diverse mesenchymal cancers with limited treatment options. Here we undertake comprehensive proteomic profiling of tumour specimens from 321 STS patients representing 11 histological subtypes. Within leiomyosarcomas, we identify three proteomic subtypes with distinct myogenesis and immune features, anatomical site distribution and survival outcomes. Characterisation of undifferentiated pleomorphic sarcomas and dedifferentiated liposarcomas with low infiltrating CD3 + T-lymphocyte levels nominates the complement cascade as a candidate immunotherapeutic target. Comparative analysis of proteomic and transcriptomic profiles highlights the proteomic-specific features for optimal risk stratification in angiosarcomas. Finally, we define functional signatures termed Sarcoma Proteomic Modules which transcend histological subtype classification and show that a vesicle transport protein signature is an independent prognostic factor for distant metastasis. Our study highlights the utility of proteomics for identifying molecular subgroups with implications for risk stratification and therapy selection and provides a rich resource for future sarcoma research.
dc.formatElectronic
dc.format.extent3834 -
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PORTFOLIO
dc.relation.ispartofNature Communications
dc.titleThe proteomic landscape of soft tissue sarcomas.
dc.typeJournal Article
dcterms.dateAccepted2023-06-15
dc.date.updated2023-07-11T07:52:31Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1038/s41467-023-39486-2
rioxxterms.licenseref.startdate2023-06-29
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37386008
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/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Systems and Precision Cancer Medicine
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)/Sarcoma Clinical Trials (R Jones) (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Functional Proteomics Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Molecular and Systems Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Endocrine Therapy Resistance
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/ImmNet
pubs.organisational-group/ICR/Students/PhD and MPhil/21/22 Starting Cohort
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1038/s41467-023-39486-2
pubs.volume14
icr.researchteamClin Trials & Stats Unit
icr.researchteamFunctional Proteomics
icr.researchteamProte & Metabolomics Fac
icr.researchteamEndocrine Therapy Resist
icr.researchteamSystems - Precision Med
icr.researchteamMol and Systems Oncology
dc.contributor.icrauthorWilding, Christopher
dc.contributor.icrauthorKrasny, Lukas
dc.contributor.icrauthorZhu, Xixuan
dc.contributor.icrauthorChadha, Madhumeeta
dc.contributor.icrauthorTam, Yuen Bun
dc.contributor.icrauthorArthur, Amani
dc.contributor.icrauthorRoumeliotis, Theodoros
dc.contributor.icrauthorChoudhary, Jyoti
dc.contributor.icrauthorSchuster, Eugene
dc.contributor.icrauthorCheang, Chon
dc.contributor.icrauthorHuang, Paul
icr.provenanceDeposited by Dr Gene Schuster on 2023-07-11. Deposit type is initial. No. of files: 1. Files: s41467-023-39486-2.pdf


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