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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-7867295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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