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The antimetastatic breast cancer activity of the viral protein‐derived peptide vCPP2319 as revealed by cellular biomechanics

dc.contributor.authorOliveira, Filipa
dc.contributor.authorCavaco, Marco
dc.contributor.authorFigueira, Tiago Nascimento
dc.contributor.authorValle, Javier
dc.contributor.authorNeves, Vera
dc.contributor.authorAndreu, David
dc.contributor.authorGaspar, Diana
dc.contributor.authorCastanho, Miguel A. R. B.
dc.date.accessioned2023-05-23T10:40:26Z
dc.date.available2023-05-23T10:40:26Z
dc.date.issued2021
dc.description© 2021 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.pt_PT
dc.description.abstractThe incidence of metastatic breast cancer (MBC) is increasing and the therapeutic arsenal available to fight it is insufficient. Brain metastases, in particular, represent a major challenge for chemotherapy as the impermeable nature of the blood–brain barrier (BBB) prevents most drugs from targeting cells in the brain. For their ability to transpose biological membranes and transport a broad spectrum of bioactive cargoes, cell-penetrating peptides (CPPs) have been hailed as ideal candidates to deliver drugs across biological barriers. A more ambitious approach is to have the CPP as a drug itself, capable of both killing cancer cells and interacting with the blood/brain interface, therefore blocking the onset of brain metastases. vCPP2319, a viral protein-derived CPP, has both properties as it: (a) is selective toward human breast cancer cells (MDA-MB-231) and increases cell stiffness compared to breast epithelial cells (MCF 10A) hindering the progression of metastases; and (b) adsorbs at the surface of human brain endothelial cells potentially counteracting metastatic cells from reaching the brain. Overall, the results reveal the selective anticancer activity of the peptide vCPP2319, which is also able to reside at the blood–brain interface, therefore counteracting brain penetration by metastatic cancer cells.pt_PT
dc.description.sponsorshipFDO, MC, and DG acknowledge FCT I.P. for fellowships PD/BD/135046/2017, PD/BD/128281/2017, and SFRH/ BPD/73500/2010. FCT I.P. is also acknowledged for funding (Projects PTDC/BIA-BQM/5027/2020 and PTDC/BBB-NAN/1578/2014). Marie Skøodowska-Curie Research and Innovation Staff Exchange (RISE) is also acknowledged for funding: call H2020-MSCARISE-2014, grant agreement 644167, 2015–2019. Work at UPF was supported by grant AGL2017-84097-C2-2-R and the “María de Maeztu” Program for Units of Excellence in R&D (MDM-2014-0370) from the Spanish Ministry of Economy and Competitiveness (MINECO).pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationThe FEBS Journal 289 (2022) 1603–1624pt_PT
dc.identifier.doi10.1111/febs.16247pt_PT
dc.identifier.eissn1742-4658
dc.identifier.issn1742-464X
dc.identifier.urihttp://hdl.handle.net/10451/57522
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherWileypt_PT
dc.relationExosomes as drug delivery systems in metastatic breast cancer
dc.relationTrans-BBB peptides for targeting brain metastasis
dc.relationSTUDYING AND DEVELOPING ANTIMICROBIAL PEPTIDE HYDROGELS USED IN TISSUE REGENERATION
dc.relationInnovative peptides against cancer and pathogenic bacteria, with advances in science, biopharmaceutical drug development, product market targeting, training , and communication.
dc.relation.publisherversionhttps://febs.onlinelibrary.wiley.com/journal/17424658pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectAnticancer activitypt_PT
dc.subjectBiomechanicspt_PT
dc.subjectBlood–brain barrierpt_PT
dc.subjectCell-penetrating peptidept_PT
dc.subjectMetastatic breast cancerpt_PT
dc.titleThe antimetastatic breast cancer activity of the viral protein‐derived peptide vCPP2319 as revealed by cellular biomechanicspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleExosomes as drug delivery systems in metastatic breast cancer
oaire.awardTitleTrans-BBB peptides for targeting brain metastasis
oaire.awardTitleSTUDYING AND DEVELOPING ANTIMICROBIAL PEPTIDE HYDROGELS USED IN TISSUE REGENERATION
oaire.awardTitleInnovative peptides against cancer and pathogenic bacteria, with advances in science, biopharmaceutical drug development, product market targeting, training , and communication.
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//PD%2FBD%2F135046%2F2017/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//PD%2FBD%2F128281%2F2017/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBPD%2F73500%2F2010/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBIA-BQM%2F5027%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/3599-PPCDT/PTDC%2FBBB-NAN%2F1578%2F2014/PT
oaire.awardURIinfo:eu-repo/grantAgreement/EC/H2020/644167/EU
oaire.citation.endPage1624pt_PT
oaire.citation.issue6pt_PT
oaire.citation.startPage1603pt_PT
oaire.citation.titleThe FEBS Journalpt_PT
oaire.citation.volume289pt_PT
oaire.fundingStream3599-PPCDT
oaire.fundingStream3599-PPCDT
oaire.fundingStreamH2020
person.familyNameOliveira
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person.familyNameGaspar
person.familyNameCastanho
person.givenNameFilipa
person.givenNameMarco
person.givenNameTiago
person.givenNameVera
person.givenNameDiana
person.givenNameMiguel
person.identifier1069324
person.identifier953259
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person.identifier.ciencia-id1412-63B8-7494
person.identifier.ciencia-id671C-1860-A160
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person.identifier.orcid0000-0002-0813-0745
person.identifier.orcid0000-0002-2989-7208
person.identifier.orcid0000-0002-9602-567X
person.identifier.orcid0000-0001-7891-7562
person.identifier.ridO-2176-2018
person.identifier.ridM-9562-2015
person.identifier.scopus-author-id26537945300
person.identifier.scopus-author-id55180303000
person.identifier.scopus-author-id56605575600
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
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project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100008530
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameEuropean Commission
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
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