| Literature DB >> 33540681 |
María Fuentes-Baile1, Elizabeth Pérez-Valenciano2, Pilar García-Morales2, Camino de Juan Romero1,2, Daniel Bello-Gil2, Víctor M Barberá1,3, Álvaro Rodríguez-Lescure4, Jesús M Sanz5, Cristina Alenda6, Miguel Saceda1,2.
Abstract
D-amino acid oxidase (DAAO) is an enzyme that catalyzes the oxidation of D-amino acids generating H2O2. 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 H2O2. 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.Entities:
Keywords: alginate capsules; cytotoxicity; enzymatic therapy; gold nanoparticle; hydrogen peroxide; magnetic nanoparticle; oxidative stress; reactive oxygen species
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Year: 2021 PMID: 33540681 PMCID: PMC7867295 DOI: 10.3390/ijms22031477
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923