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NET models meeting 2024: the current state of neuroendocrine tumour research models and our future aspirations

cris.virtual.author-orcid
cris.virtual.author-orcid0000-0002-8941-7990
cris.virtualsource.author-orcid8596fee5-4d7b-45b0-89f4-b464fac81857
cris.virtualsource.author-orcidc1e81d19-bff9-41a4-9319-ff4897222d31
cris.virtualsource.author-orcidd859b62c-b0dc-4c81-8824-f971a2ff907f
cris.virtualsource.author-orcide626131f-a7df-4cb3-9a66-3c34be7eacd9
datacite.rightsopen.access
dc.contributor.authorEar, Po Hien
dc.contributor.authorMarinoni, Ilaria
dc.contributor.authorDayton, Talya
dc.contributor.authorGuenter, Rachael
dc.contributor.authorQuelle, Dawn
dc.contributor.authorBattistella, Anna
dc.contributor.authorBuishand, Floryne O
dc.contributor.authorChittaranjan, Suganthi
dc.contributor.authorDu, Yi-Cheih Nancy
dc.contributor.authorMarques, Ines
dc.contributor.authorPellegata, Natalia
dc.contributor.authorSadowski, Samira Mercedes
dc.contributor.authorTirosh, Amit
dc.contributor.authorApril-Monn, Simon
dc.contributor.authorAurilia, Cinzia
dc.contributor.authorJaskula-Sztul, Renata
dc.contributor.authorBaena Moreno, Maria Jesús
dc.contributor.authorDonati, Simone
dc.contributor.authorEnglish, Katherine A
dc.contributor.authorHernandez Llorens, Maria A.
dc.contributor.authorHodgetts, Harry
dc.contributor.authorMarini, Francesca
dc.contributor.authorMartins, Maria
dc.contributor.authorPalmini, Gaia
dc.contributor.authorSoldevilla, Beatriz
dc.contributor.authorSchrader, Jörg
dc.contributor.authorThakker, Rajesh V
dc.contributor.authorLines, Kate E
dc.date.accessioned2024-12-20T11:38:09Z
dc.date.available2024-12-20T11:38:09Z
dc.date.issued2024
dc.description.abstractCurrent models for the study of neuroendocrine tumours (NETs) are severely limited. While in vitro (e.g. cell lines), ex vivo (e.g. organoids), and in vivo (e.g. mice) models all exist, each has limitations. To address these limitations and collectively identify strategies to move the NET models field forward, we held an inaugural NET Models meeting, hosted by our founding group: Dr. Lines (Oxford); Prof. Quelle (Iowa); Dr. Dayton (Barcelona); Dr. Ear (Iowa); Dr. Marinoni (Bern); and Dr. Guenter (Alabama). This 2-day meeting in Oxford (UK) was organised and supported by Bioscientifica Ltd and was solely dedicated to the discussion of NET models. The meeting was attended by 30 international researchers (from UK, EU, Israel, USA and Canada). Plenary talks were given by Prof. Thakker who summarised NET research over the last few decades, and Dr. Schrader who described the process and pitfalls of generating new cell lines. Eight researchers also presented their work on topics ranging from human cell 3D bioprinting, to zebrafish models, and included novel ideas as well as improvements on current concepts. This was followed by an interactive workshop where discussion topics included, a summary of currently available NET models, limitations of these models, barriers to developing new models, and how we can address these issues going forward. This white paper summarises the key points raised in these discussions, as well as the future aspirations of the NET Models Consortium. The next meeting will take place in Oxford (UK) in 2025, contact contact@netcancerfoundation.com for more information.
dc.description.sponsorshipInstitut für Gewebemedizin und Pathologie - Labor Endokrine Pathologie
dc.description.sponsorshipInstitute of Anatomy, Developmental Biology and Regeneration
dc.identifier.doi10.48620/78672
dc.identifier.pmid39822778
dc.identifier.publisherDOI10.1530/EO-24-0055
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/194391
dc.language.isoen
dc.publisherBioscientifica
dc.relation.ispartofEndocrine Oncology
dc.relation.issn2634-4793
dc.titleNET models meeting 2024: the current state of neuroendocrine tumour research models and our future aspirations
dc.typearticle
dspace.entity.typePublication
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oaire.citation.issue1
oaire.citation.volume4
oairecerif.author.affiliationInstitut für Gewebemedizin und Pathologie - Labor Endokrine Pathologie
oairecerif.author.affiliationInstitute of Anatomy, Developmental Biology and Regeneration
oairecerif.author.affiliation2Institute of Tissue Medicine and Pathology, Endocrine Pathology
oairecerif.author.affiliation2Institute of Anatomy
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unibe.subtype.articlereview

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