CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells
D-amino acid oxidase (DAAO) catalyzes the oxidation of D-amino acids generating hydrogen peroxide, a potential producer of reactive oxygen species. In this study, we used a CLytA-DAAO chimera, both free and bound to magnetic nanoparticles, against colon carcinoma, pancreatic adenocarcinoma, and glio...
| Autores: | , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universidad Complutense de Madrid (UCM) |
| Repositorio: | Docta Complutense |
| Idioma: | inglés |
| OAI Identifier: | oai:docta.ucm.es:20.500.14352/94062 |
| Acceso en línea: | https://hdl.handle.net/20.500.14352/94062 |
| Access Level: | acceso abierto |
| Palabra clave: | Biología molecular (Biología) 2403 Bioquímica |
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CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cellsFuentes-Baile, MaríaBello-Gil, DanielPérez-Valenciano, ElizabethSanz, JesúsGarcía-Morales, PilarMaestro García-Donas, María BeatrizVentero, MaríaAlenda, CristinaBarberá, VictorSaceda, ManuelBiología molecular (Biología)2403 BioquímicaD-amino acid oxidase (DAAO) catalyzes the oxidation of D-amino acids generating hydrogen peroxide, a potential producer of reactive oxygen species. In this study, we used a CLytA-DAAO chimera, both free and bound to magnetic nanoparticles, against colon carcinoma, pancreatic adenocarcinoma, and glioblastoma cell lines. We found that the enzyme induces cell death in most of the cell lines tested and its efficiency increases significantly when it is immobilized in nanoparticles. We also tested this enzyme therapy in non-tumor cells, and we found that there is not cell death induction, or it is significantly lower than in tumor cells. The mechanism triggering cell death is apparently a classical apoptosis pathway in the glioblastoma cell lines, while in colon and pancreatic carcinoma cell lines, CLytA-DAAO-induced cell death is a necrosis. Our results constitute a proof of concept that an enzymatic therapy, based on magnetic nanoparticles-delivering CLytA-DAAO, could constitute a useful therapy against cancer and besides it could be used as an enhancer of other treatments such as epigenetic therapy, radiotherapy, and treatments based on DNA repair.Universidad Complutense de Madrid20202020-01-0120202020-01-01journal articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/20.500.14352/94062reponame:Docta Complutenseinstname:Universidad Complutense de Madrid (UCM)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:docta.ucm.es:20.500.14352/940622026-06-02T12:44:21Z |
| dc.title.none.fl_str_mv |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| title |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| spellingShingle |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells Fuentes-Baile, María Biología molecular (Biología) 2403 Bioquímica |
| title_short |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| title_full |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| title_fullStr |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| title_full_unstemmed |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| title_sort |
CLytA-DAAO, free and immobilized in magnetic nanoparticles, induces cell death in human cancer cells |
| dc.creator.none.fl_str_mv |
Fuentes-Baile, María Bello-Gil, Daniel Pérez-Valenciano, Elizabeth Sanz, Jesús García-Morales, Pilar Maestro García-Donas, María Beatriz Ventero, María Alenda, Cristina Barberá, Victor Saceda, Manuel |
| author |
Fuentes-Baile, María |
| author_facet |
Fuentes-Baile, María Bello-Gil, Daniel Pérez-Valenciano, Elizabeth Sanz, Jesús García-Morales, Pilar Maestro García-Donas, María Beatriz Ventero, María Alenda, Cristina Barberá, Victor Saceda, Manuel |
| author_role |
author |
| author2 |
Bello-Gil, Daniel Pérez-Valenciano, Elizabeth Sanz, Jesús García-Morales, Pilar Maestro García-Donas, María Beatriz Ventero, María Alenda, Cristina Barberá, Victor Saceda, Manuel |
| author2_role |
author author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Universidad Complutense de Madrid |
| dc.subject.none.fl_str_mv |
Biología molecular (Biología) 2403 Bioquímica |
| topic |
Biología molecular (Biología) 2403 Bioquímica |
| description |
D-amino acid oxidase (DAAO) catalyzes the oxidation of D-amino acids generating hydrogen peroxide, a potential producer of reactive oxygen species. In this study, we used a CLytA-DAAO chimera, both free and bound to magnetic nanoparticles, against colon carcinoma, pancreatic adenocarcinoma, and glioblastoma cell lines. We found that the enzyme induces cell death in most of the cell lines tested and its efficiency increases significantly when it is immobilized in nanoparticles. We also tested this enzyme therapy in non-tumor cells, and we found that there is not cell death induction, or it is significantly lower than in tumor cells. The mechanism triggering cell death is apparently a classical apoptosis pathway in the glioblastoma cell lines, while in colon and pancreatic carcinoma cell lines, CLytA-DAAO-induced cell death is a necrosis. Our results constitute a proof of concept that an enzymatic therapy, based on magnetic nanoparticles-delivering CLytA-DAAO, could constitute a useful therapy against cancer and besides it could be used as an enhancer of other treatments such as epigenetic therapy, radiotherapy, and treatments based on DNA repair. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 2020-01-01 2020 2020-01-01 |
| dc.type.none.fl_str_mv |
journal article http://purl.org/coar/resource_type/c_6501 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/20.500.14352/94062 |
| url |
https://hdl.handle.net/20.500.14352/94062 |
| dc.language.none.fl_str_mv |
Inglés eng |
| language_invalid_str_mv |
Inglés |
| language |
eng |
| dc.rights.none.fl_str_mv |
open access http://purl.org/coar/access_right/c_abf2 |
| dc.rights.openaire.fl_str_mv |
info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.source.none.fl_str_mv |
reponame:Docta Complutense instname:Universidad Complutense de Madrid (UCM) |
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Universidad Complutense de Madrid (UCM) |
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Docta Complutense |
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Docta Complutense |
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