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dc.date.accessioned 2023-12-29T18:14:44Z
dc.date.available 2023-12-29T18:14:44Z
dc.date.issued 2019-03-18
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/162149
dc.description.abstract Nuclear localization signals are short amino acid sequences that target proteins for nuclear import. In this manuscript, we have generated a chimeric tri-functional peptide composed of a cell penetrating peptide (CPP), a nuclear localization sequence and an interfering peptide blocking the interaction between TEAD and YAP, two transcription factors involved in the Hippo signalling pathway, whose deregulation is related to several types of cancer. We have validated the cell penetration and nuclear localization by flow cytometry and fluorescence microscopy and shown that the new generated peptide displays an apoptotic effect in tumor cell lines thanks to the specific nuclear delivery of the cargo, which targets a protein/protein interaction in the nucleus. In addition, the peptide has an anti-tumoral effect in vivo in xenograft models of breast cancer. The chimeric peptide designed in the current study shows encouraging prospects for developing nuclear anti- neoplastic drugs. en
dc.language es es
dc.title New Therapeutic Approach for Targeting Hippo Signalling Pathway en
dc.type Articulo es
sedici.identifier.other https://doi.org/10.1038/s41598-019-41404-w es
sedici.creator.person Domínguez Berrocal, Leticia es
sedici.creator.person Cirri, Erica es
sedici.creator.person Zhang, Xiguang es
sedici.creator.person Andrini, Laura Beatriz es
sedici.creator.person Marín, Gustavo Horacio es
sedici.creator.person Lebel-Binay, Sophie es
sedici.creator.person Rebollo, Angelita es
sedici.subject.materias Ciencias Médicas es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Médicas es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Scientific Reports es
sedici.relation.journalVolumeAndIssue vol. 9 es


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