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CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?

D-amino acid oxidase (DAAO) is an enzyme that catalyzes the oxidation of D-amino acids generating H(2)O(2). The enzymatic chimera formed by DAAO bound to the choline-binding domain of N-acetylmuramoyl-L-alanine amidase (CLytA) induces cytotoxicity in several pancreatic and colorectal carcinoma and g...

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Autores principales: Fuentes-Baile, María, Pérez-Valenciano, Elizabeth, García-Morales, Pilar, de Juan Romero, Camino, Bello-Gil, Daniel, Barberá, Víctor M., Rodríguez-Lescure, Álvaro, Sanz, Jesús M., Alenda, Cristina, Saceda, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867295/
https://www.ncbi.nlm.nih.gov/pubmed/33540681
http://dx.doi.org/10.3390/ijms22031477
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author Fuentes-Baile, María
Pérez-Valenciano, Elizabeth
García-Morales, Pilar
de Juan Romero, Camino
Bello-Gil, Daniel
Barberá, Víctor M.
Rodríguez-Lescure, Álvaro
Sanz, Jesús M.
Alenda, Cristina
Saceda, Miguel
author_facet Fuentes-Baile, María
Pérez-Valenciano, Elizabeth
García-Morales, Pilar
de Juan Romero, Camino
Bello-Gil, Daniel
Barberá, Víctor M.
Rodríguez-Lescure, Álvaro
Sanz, Jesús M.
Alenda, Cristina
Saceda, Miguel
author_sort Fuentes-Baile, María
collection PubMed
description D-amino acid oxidase (DAAO) is an enzyme that catalyzes the oxidation of D-amino acids generating H(2)O(2). The enzymatic chimera formed by DAAO bound to the choline-binding domain of N-acetylmuramoyl-L-alanine amidase (CLytA) induces cytotoxicity in several pancreatic and colorectal carcinoma and glioblastoma cell models. In the current work, we determined whether the effect of CLytA-DAAO immobilized in magnetic nanoparticles, gold nanoparticles, and alginate capsules offered some advantages as compared to the free CLytA-DAAO. Results indicate that the immobilization of CLytA-DAAO in magnetic nanoparticles increases the stability of the enzyme, extending its time of action. Besides, we compared the effect induced by CLytA-DAAO with the direct addition of hydrogen peroxide, demonstrating that the progressive generation of reactive oxygen species by CLytA-DAAO is more effective in inducing cytotoxicity than the direct addition of H(2)O(2). Furthermore, a pilot study has been initiated in biopsies obtained from pancreatic and colorectal carcinoma and glioblastoma patients to evaluate the expression of the main genes involved in resistance to CLytA-DAAO cytotoxicity. Based on our findings, we propose that CLytA-DAAO immobilized in magnetic nanoparticles could be effective in a high percentage of patients and, therefore, be used as an anti-cancer therapy for pancreatic and colorectal carcinoma and glioblastoma.
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spelling pubmed-78672952021-02-07 CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients? Fuentes-Baile, María Pérez-Valenciano, Elizabeth García-Morales, Pilar de Juan Romero, Camino Bello-Gil, Daniel Barberá, Víctor M. Rodríguez-Lescure, Álvaro Sanz, Jesús M. Alenda, Cristina Saceda, Miguel Int J Mol Sci Article D-amino acid oxidase (DAAO) is an enzyme that catalyzes the oxidation of D-amino acids generating H(2)O(2). The enzymatic chimera formed by DAAO bound to the choline-binding domain of N-acetylmuramoyl-L-alanine amidase (CLytA) induces cytotoxicity in several pancreatic and colorectal carcinoma and glioblastoma cell models. In the current work, we determined whether the effect of CLytA-DAAO immobilized in magnetic nanoparticles, gold nanoparticles, and alginate capsules offered some advantages as compared to the free CLytA-DAAO. Results indicate that the immobilization of CLytA-DAAO in magnetic nanoparticles increases the stability of the enzyme, extending its time of action. Besides, we compared the effect induced by CLytA-DAAO with the direct addition of hydrogen peroxide, demonstrating that the progressive generation of reactive oxygen species by CLytA-DAAO is more effective in inducing cytotoxicity than the direct addition of H(2)O(2). Furthermore, a pilot study has been initiated in biopsies obtained from pancreatic and colorectal carcinoma and glioblastoma patients to evaluate the expression of the main genes involved in resistance to CLytA-DAAO cytotoxicity. Based on our findings, we propose that CLytA-DAAO immobilized in magnetic nanoparticles could be effective in a high percentage of patients and, therefore, be used as an anti-cancer therapy for pancreatic and colorectal carcinoma and glioblastoma. MDPI 2021-02-02 /pmc/articles/PMC7867295/ /pubmed/33540681 http://dx.doi.org/10.3390/ijms22031477 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fuentes-Baile, María
Pérez-Valenciano, Elizabeth
García-Morales, Pilar
de Juan Romero, Camino
Bello-Gil, Daniel
Barberá, Víctor M.
Rodríguez-Lescure, Álvaro
Sanz, Jesús M.
Alenda, Cristina
Saceda, Miguel
CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title_full CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title_fullStr CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title_full_unstemmed CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title_short CLytA-DAAO Chimeric Enzyme Bound to Magnetic Nanoparticles. A New Therapeutical Approach for Cancer Patients?
title_sort clyta-daao chimeric enzyme bound to magnetic nanoparticles. a new therapeutical approach for cancer patients?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867295/
https://www.ncbi.nlm.nih.gov/pubmed/33540681
http://dx.doi.org/10.3390/ijms22031477
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