dc.contributor.author | Tellez Gabriel, Marta | |
dc.contributor.author | Cochonneau, Denis | |
dc.contributor.author | Jubelin, Camille | |
dc.contributor.author | Heymann, Marie-Françoise | |
dc.contributor.author | Heymann, Dominique | |
dc.date.accessioned | 2019-10-11T08:58:44Z | |
dc.date.available | 2019-10-11T08:58:44Z | |
dc.date.issued | 2018-12-24 | |
dc.description.abstract | The main cause of death from cancer is associated with the development of metastases, resulting from the inability of current therapies to cure patients at metastatic stages. Generating preclinical models to better characterize the evolution of the disease is thus of utmost importance, in order to implement effective new cancer biomarkers and therapies. Circulating Tumor Cells (CTCs) are good candidates for generating preclinical models, making it possible to follow up the spatial and temporal heterogeneity of tumor tissues. This method is a non-invasive liquid biopsy that can be obtained at any stage of the disease. It partially summarizes the molecular heterogeneity of the corresponding tumors at a given time. Here, we discuss the CTC-derived models that have been generated so far, from simplified 2D cultures to the most complex CTC-derived explants (CDX models). We highlight the challenges and strengths of these preclinical tools, as well as some of the recent studies published using these models. | en_US |
dc.description.sponsorship | Bone Cancer Research Trust (UK)
Fondation de l’Avenir (France) | en_US |
dc.description | Source at <a href=https://doi.org/10.3390/cancers11010019>https://doi.org/10.3390/cancers11010019</a> | en_US |
dc.identifier.citation | Tellez-Gabriel, M., Cochonneau, D., Cadé, M., Jubelin, C., Heymann, M.F. & Heymann, D. (2019). Circulating tumor cell-derived pre-clinical models for personalized medicine. <i>Cancers, 11</i>(1), 19. https://doi.org/10.3390/cancers11010019 | en_US |
dc.identifier.cristinID | FRIDAID 1699747 | |
dc.identifier.doi | 10.3390/cancers11010019 | |
dc.identifier.issn | 2072-6694 | |
dc.identifier.uri | https://hdl.handle.net/10037/16375 | |
dc.language.iso | eng | en_US |
dc.publisher | MDPI | en_US |
dc.relation.journal | Cancers | |
dc.rights.accessRights | openAccess | en_US |
dc.subject | VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Oncology: 762 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762 | en_US |
dc.subject | VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Clinical pharmacology: 739 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Klinisk farmakologi: 739 | en_US |
dc.subject | circulating tumor cells | en_US |
dc.subject | spheroids | en_US |
dc.subject | organoids | en_US |
dc.subject | preclinical models | en_US |
dc.subject | tumor heterogeneity | en_US |
dc.subject | personalized medicine | en_US |
dc.title | Circulating tumor cell-derived pre-clinical models for personalized medicine | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |