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dc.contributor.authorRodriguez-Martinez, Alba
dc.contributor.authorSimon-Saez, Iris 
dc.contributor.authorPerales, Sonia
dc.contributor.authorGarrido-Navas, Carmen
dc.contributor.authorRusso, Alessandro
dc.contributor.authorMiguel-Perez, Diego
dc.contributor.authorPuche-Sanz, Ignacio
dc.contributor.authorAlaminos, Clara
dc.contributor.authorCeron, Jorge
dc.contributor.authorLorente Acosta, José Antonio 
dc.contributor.authorMolina, María Pilar
dc.contributor.authorGonzalez, Coral
dc.contributor.authorCristofanilli, Massimo
dc.contributor.authorOrtigosa-Palomo, Alba
dc.contributor.authorRolfo, Christian
dc.contributor.authorSerrano, María José
dc.contributor.authorReal Luna, Pedro José 
dc.date.accessioned2025-01-21T11:09:24Z
dc.date.available2025-01-21T11:09:24Z
dc.date.issued2022-02-07
dc.identifier.urihttps://hdl.handle.net/10481/99827
dc.description.abstractBackground: Platelets are active players in tumorigenesis, although the exact interactive mechanisms and their direct impact on tumor cells remain largely unknown. Methods: Bidirectional transference of lipids, proteins and RNA between platelets and tumor cells and its impact on tumor cell behavior and tumor process are analyzed in this work. Phenotypic, genetic and functional modifications induced by platelets were analyzed both in tumor cell lines and in circulating tumor cells (CTCs). Results: Data from these assays showed that platelets transferred structural components to tumor cells with higher efficiency than tumor cells to platelets (p = 0.001). This biological interplay occurred by direct contact, internalization or via extracellular vesicles. As a result, tumor cells acquired platelet markers (CD61 and CD42), showed decreased EpCAM, expressed epithelial-to-mesenchymal transition markers, and increased proliferation rates. Moreover, we were able to detect CD61 in CTCs from early and advanced prostate cancer. Conclusions: Our results demonstrated, for the first time, that platelets educate tumor cells by highly efficient transference of lipids, proteins and RNA through different mechanisms. These results suggest that tumor cells and CTCs might acquire highly dynamic and aggressive phenotypes due to platelets interaction including EMT, stem-like phenotype and high proliferative rates.es_ES
dc.description.sponsorshipThis work was supported by ISCIII Health Research Institute (P17/00989), 'La Caixa' Foundationes_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectPlateletses_ES
dc.subjectCirculating tumor cells (CTCs)es_ES
dc.subjectPlatelet-educated tumors (PETs)es_ES
dc.subjectEpithelial-to-mesenchymal transition (EMT)es_ES
dc.subjectCD61es_ES
dc.subjectPlaquetas es_ES
dc.subjectCélulas Tumorales Circulantes (CTCs)es_ES
dc.subjectPlaquetas educadas por el tumores_ES
dc.subjectTransición Epitelio Mesénquimaes_ES
dc.titleExchange of cellular components between platelets and tumor cells: impact on tumor cells behaviores_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.7150/thno.64252
dc.type.hasVersionAMes_ES


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