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dc.date.accessioned2020-05-06T19:46:38Z
dc.date.available2020-05-06T19:46:38Z
dc.date.created2019-07-25T11:41:29Z
dc.date.issued2019
dc.identifier.citationvan IJzendoorn, David G.P. Szuhai, Karoly Briaire-De Bruijn, Inge H Kostine, Marie Kuijjer, Marieke Lydia Bovée, Judith V.M.G. . Machine learning analysis of gene expression data reveals novel diagnostic and prognostic biomarkers and identifies therapeutic targets for soft tissue sarcomas. PLoS Computational Biology. 2019, 15(2), 1-19
dc.identifier.urihttp://hdl.handle.net/10852/75198
dc.description.abstractBased on morphology it is often challenging to distinguish between the many different soft tissue sarcoma subtypes. Moreover, outcome of disease is highly variable even between patients with the same disease. Machine learning on transcriptome sequencing data could be a valuable new tool to understand differences between and within entities. Here we used machine learning analysis to identify novel diagnostic and prognostic markers and therapeutic targets for soft tissue sarcomas. Gene expression data was used from the Cancer Genome Atlas, the Genotype-Tissue Expression project and the French Sarcoma Group. We identified three groups of tumors that overlap in their molecular profiles as seen with unsupervised t-Distributed Stochastic Neighbor Embedding clustering and a deep neural network. The three groups corresponded to subtypes that are morphologically overlapping. Using a random forest algorithm, we identified novel diagnostic markers for soft tissue sarcoma that distinguished between synovial sarcoma and MPNST, and that we validated using qRT-PCR in an independent series. Next, we identified prognostic genes that are strong predictors of disease outcome when used in a k-nearest neighbor algorithm. The prognostic genes were further validated in expression data from the French Sarcoma Group. One of these, HMMR, was validated in an independent series of leiomyosarcomas using immunohistochemistry on tissue micro array as a prognostic gene for disease-free interval. Furthermore, reconstruction of regulatory networks combined with data from the Connectivity Map showed, amongst others, that HDAC inhibitors could be a potential effective therapy for multiple soft tissue sarcoma subtypes. A viability assay with two HDAC inhibitors confirmed that both leiomyosarcoma and synovial sarcoma are sensitive to HDAC inhibition. In this study we identified novel diagnostic markers, prognostic markers and therapeutic leads from multiple soft tissue sarcoma gene expression datasets. Thus, machine learning algorithms are powerful new tools to improve our understanding of rare tumor entities.
dc.languageEN
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMachine learning analysis of gene expression data reveals novel diagnostic and prognostic biomarkers and identifies therapeutic targets for soft tissue sarcomas
dc.typeJournal article
dc.creator.authorvan IJzendoorn, David G.P.
dc.creator.authorSzuhai, Karoly
dc.creator.authorBriaire-De Bruijn, Inge H
dc.creator.authorKostine, Marie
dc.creator.authorKuijjer, Marieke Lydia
dc.creator.authorBovée, Judith V.M.G.
cristin.unitcode185,57,55,0
cristin.unitnameMarieke Kuijjer Group - Computational Biology and Systems Medicine
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1712666
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS Computational Biology&rft.volume=15&rft.spage=1&rft.date=2019
dc.identifier.jtitlePLoS Computational Biology
dc.identifier.volume15
dc.identifier.issue2
dc.identifier.doihttps://doi.org/10.1371/journal.pcbi.1006826
dc.identifier.urnURN:NBN:no-78280
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn1553-734X
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/75198/1/2019-02-21_van_ijzendoorn_plos_compbio.pdf
dc.type.versionPublishedVersion
cristin.articleide1006826
dc.relation.projectNFR/187615


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