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Functionalized immunostimulating complexes with protein A via lipid vinyl sulfones to deliver cancer drugs to trastuzumab-resistant HER2-overexpressing breast cancer cells.

dc.contributor.authorRodríguez-Serrano, Fernando
dc.contributor.authorMut-Salud, Nuria
dc.contributor.authorCruz-Bustos, Teresa
dc.contributor.authorGomez-Samblas, Mercedes
dc.contributor.authorCarrasco, Esther
dc.contributor.authorGarrido, Jose Manuel
dc.contributor.authorLópez-Jaramillo, F Javier
dc.contributor.authorSantoyo-Gonzalez, Francisco
dc.contributor.authorOsuna, Antonio
dc.date.accessioned2023-01-25T08:37:26Z
dc.date.available2023-01-25T08:37:26Z
dc.date.issued2016-09-19
dc.description.abstractAround 20%-30% of breast cancers overexpress the proto-oncogene human epidermal growth receptor 2 (HER2), and they are characterized by being very invasive. Therefore, many current studies are focused on testing new therapies against tumors that overexpress this receptor. In particular, there exists major interest in new strategies to fight breast cancer resistant to trastuzumab (Tmab), a humanized antibody that binds specifically to HER2 interfering with its mitogenic signaling. Our team has previously developed immunostimulating complexes (ISCOMs) as nanocapsules functionalized with lipid vinyl sulfones, which can incorporate protein A and bind to G immunoglobulins that makes them very flexible nanocarriers. The aim of this in vitro study was to synthesize and evaluate a drug delivery system based on protein A-functionalized ISCOMs to target HER2-overexpressing cells. We describe the preparation of ISCOMs, the loading with the drugs doxorubicin and paclitaxel, the binding of ISCOMs to alkyl vinyl sulfone-protein A, the coupling of Tmab, and the evaluation in both HER2-overexpressing breast cancer cells (HCC1954) and non-overexpressing cells (MCF-7) by flow cytometry and fluorescence microscopy. Results show that the uptake is dependent on the level of overexpression of HER2, and the analysis of the cell viability reveals that targeted drugs are selective toward HCC1954, whereas MCF-7 cells remain unaffected. Protein A-functionalized ISCOMs are versatile carriers that can be coupled to antibodies that act as targeting agents to deliver drugs. When coupling to Tmab and loading with paclitaxel or doxorubicin, they become efficient vehicles for the selective delivery of the drug to Tmab-resistant HER2-overexpressing breast cancer cells. These nanoparticles may pave the way for the development of novel therapies for poor prognosis resistant patients.
dc.identifier.doi10.2147/IJN.S112560
dc.identifier.essn1178-2013
dc.identifier.pmcPMC5034911
dc.identifier.pmid27698563
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034911/pdf
dc.identifier.unpaywallURLhttps://www.dovepress.com/getfile.php?fileID=32490
dc.identifier.urihttp://hdl.handle.net/10668/10500
dc.journal.titleInternational journal of nanomedicine
dc.journal.titleabbreviationInt J Nanomedicine
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.page.number4777-4785
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectHER2
dc.subjectdoxorubicin
dc.subjectnanoparticle
dc.subjectpaclitaxel
dc.subjectprotein A
dc.subjecttargeted drug delivery
dc.subjecttrastuzumab
dc.subject.meshAntineoplastic Agents
dc.subject.meshBreast Neoplasms
dc.subject.meshCell Death
dc.subject.meshCell Line, Tumor
dc.subject.meshCell Survival
dc.subject.meshDoxorubicin
dc.subject.meshDrug Delivery Systems
dc.subject.meshDrug Resistance, Neoplasm
dc.subject.meshEndocytosis
dc.subject.meshFemale
dc.subject.meshFlow Cytometry
dc.subject.meshHumans
dc.subject.meshISCOMs
dc.subject.meshLipids
dc.subject.meshMCF-7 Cells
dc.subject.meshNanoparticles
dc.subject.meshOxazines
dc.subject.meshPaclitaxel
dc.subject.meshProto-Oncogene Mas
dc.subject.meshReceptor, ErbB-2
dc.subject.meshStaphylococcal Protein A
dc.subject.meshSulfones
dc.subject.meshTrastuzumab
dc.titleFunctionalized immunostimulating complexes with protein A via lipid vinyl sulfones to deliver cancer drugs to trastuzumab-resistant HER2-overexpressing breast cancer cells.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication

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