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 O . 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 gliob...

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Published in:International journal of molecular sciences Vol. 22; no. 3; p. 1477
Main Authors: 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
Format: Journal Article
Language:English
Published: Switzerland MDPI AG 02-02-2021
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Summary:D-amino acid oxidase (DAAO) is an enzyme that catalyzes the oxidation of D-amino acids generating H O . 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 O . 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.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms22031477