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Preclinical models of breast cancer: b6bc, a transplantable hormone receptor-positive c57bl/6 mouse cell line

dc.contributor.authorPérez Lanzon, María
dc.contributor.authorMaiuri, M. C.
dc.contributor.authorLópez Otín, Carlos 
dc.contributor.authorKroemer, G.
dc.date.accessioned2024-07-11T07:34:14Z
dc.date.available2024-07-11T07:34:14Z
dc.date.issued2024
dc.identifier.citationGenes and Immunity (2024); doi:10.1038/s41435-023-00241-8
dc.identifier.issn1466-4879
dc.identifier.urihttps://hdl.handle.net/10651/73693
dc.description.abstractPreclinical animal models are essential tools to develop and evaluate new anticancer treatments, notably immunotherapies, in which the complex interactions between cancer cells and the immune system need to be recapitulated. Consequently, the degree to which the preclinical model mimics certain disease aspects likely conditions its clinical translatability. In the context of breast cancer (BC), representative models should mimic key disease features such as the hormone receptor and ERBB2 status, as well as the composition of the tumor immune infiltrate. However, such information is generally limited notably for transplantable mouse cancer cell lines, which tend to be poorly characterized with respect to their histopathological subtype and to the tumor microenvironment that they generate, especially if they fail to strive after injection into syngeneic hosts [1].
dc.language.isoeng
dc.relation.ispartofGenes and Immunity
dc.rights© 2025 Springer Nature
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85182172289&doi=10.1038%2fs41435-023-00241-8&partnerID=40&md5=dd9cda8f76c45a8310e63633bfbda6ec
dc.titlePreclinical models of breast cancer: b6bc, a transplantable hormone receptor-positive c57bl/6 mouse cell line
dc.typejournal article
dc.identifier.doi10.1038/s41435-023-00241-8
dc.relation.publisherversionhttp://dx.doi.org/10.1038/s41435-023-00241-8


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