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dc.contributor.authorFuente Vivas, Dalia de la 
dc.contributor.authorCasar, Berta
dc.contributor.authorCrespo, Piero
dc.date.accessioned2026-10-07T07:56:33Z
dc.date.available2026-10-07T07:56:33Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/10259/12239
dc.descriptionPóster presentado en: EACR 2021 Virtual Congress, 9-12 June 2021en
dc.description.abstractActivation of the Ras-ERK signaling cascade is associated with increased metastasis risk inbreast cancer. In the present study. ERK dimerization plays a crucial role in the migrationand invasion of breast tumor cells. ERK dimers bind to the scaffold protein KSR1 toenhance migration. Blocking ERK dimers formation reduced invasion capacity of MCF-7and MDA-231-MB tumors cells. Thus, targeting ERK dimerization could emerge as a validtherapeutic strategy for the treatment of breast cancer.en
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.subject.otherTumoreses
dc.subject.otherTumorsen
dc.subject.otherCélulas cancerosases
dc.subject.otherCancer cellsen
dc.titleERK dimerization promotes migration and invasionen
dc.typeinfo:eu-repo/semantics/conferenceObjectes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersiones


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