Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/145235
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dc.creatorCarvalho, AS
dc.creatorMoraes, MCS
dc.creatorNa, CH
dc.creatorFierro-Monti, I
dc.creatorHenriques, A
dc.creatorZahedi, S
dc.creatorBodo, C
dc.creatorTranfield, EM
dc.creatorSousa, AL
dc.creatorFarinho, A
dc.creatorRodrigues, LV
dc.creatorPinto, P
dc.creatorBárbara, C
dc.creatorMota, L
dc.creatorAbreu, TT
dc.creatorSemedo, J
dc.creatorSeixas, S
dc.creatorKumar, P
dc.creatorCosta-Silva, B
dc.creatorPandey, A
dc.creatorMatthiesen, R
dc.date.accessioned2022-11-17T11:32:46Z-
dc.date.available2022-11-17T11:32:46Z-
dc.date.issued2020
dc.identifier.issn2072-6694
dc.identifier.urihttps://hdl.handle.net/10216/145235-
dc.description.abstractAcellular bronchoalveolar lavage (BAL) proteomics can partially separate lung cancer from non-lung cancer patients based on principal component analysis and multivariate analysis. Furthermore, the variance in the proteomics data sets is correlated mainly with lung cancer status and, to a lesser extent, smoking status and gender. Despite these advances BAL small and large extracellular vehicles (EVs) proteomes reveal aberrant protein expression in paracrine signaling mechanisms in cancer initiation and progression. We consequently present a case-control study of 24 bronchoalveolar lavage extracellular vesicle samples which were analyzed by state-of-the-art liquid chromatography-mass spectrometry (LC-MS). We obtained evidence that BAL EVs proteome complexity correlated with lung cancer stage 4 and mortality within two years´ follow-up (p value = 0.006). The potential therapeutic target DNMT3B complex is significantly up-regulated in tumor tissue and BAL EVs. The computational analysis of the immune and fibroblast cell markers in EVs suggests that patients who deceased within the follow-up period display higher marker expression indicative of innate immune and fibroblast cells (four out of five cases). This study provides insights into the proteome content of BAL EVs and their correlation to clinical outcomes.
dc.description.sponsorshipR.M. is supported by Fundação para a Ciência e a Tecnologia (CEEC position, 2019–2025 investigator). This article is a result of the projects (iNOVA4Health—UID/Multi/04462/2013), supported by Lisboa Portugal Regional Operational Programme (Lisboa2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). This work is also funded by FEDER funds through the COMPETE 2020 Programme and National Funds through FCT—Portuguese Foundation for Science and Technology under the projects number PTDC/BTM-TEC/30087/2017 and PTDC/BTM-TEC/30088/2017. This work was supported by the Wellcome Trust/DBT India Alliance Margdarshi Fellowship (grant number IA/M/15/1/502023) awarded to A.P. B.C.-S., M.C.S.C. and C.B. are supported by the Champalimaud Foundation and the EMBO Installation Grant 3921.
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FMulti%2F04462%2F2013/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBTM-TEC%2F30087%2F2017/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC%2FBTM-TEC%2F30088%2F2017/PT
dc.relation.ispartofCancers, vol.12(11):3450
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBronchoalveolar lavage
dc.subjectExtracellular vesicles
dc.subjectImmuno oncology
dc.subjectLung cancer
dc.subjectProteomics
dc.titleIs the proteome of bronchoalveolar lavage extracellular vesicles a marker of advanced lung cancer?
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/cancers12113450
dc.relation.publisherversionhttps://www.mdpi.com/2072-6694/12/11/3450
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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