Application of Gold Nanoparticles as Radiosensitizer for Metastatic Prostate Cancer Cell Lines

Author:

Soares Sílvia123456,Faria Isabel7ORCID,Aires Fátima8ORCID,Monteiro Armanda8,Pinto Gabriela8,Sales Maria Goreti159ORCID,Correa-Duarte Miguel A.1011ORCID,Guerreiro Susana G.31213ORCID,Fernandes Rúben2314ORCID

Affiliation:

1. ICBAS—School of Medicine and Biomedical Sciences, University of Porto, 4050-313 Porto, Portugal

2. FP-I3ID, FP-BHS, Universidade Fernando Pessoa (UFP), 4249-004 Porto, Portugal

3. Instituto de Investigação e Inovação em Saúde (i3S), 4200-135 Porto, Portugal

4. Faculty of Chemistry, University of Vigo, 36310 Vigo, Spain

5. CEB, Centre of Biological Engineering of Minho University, 4710-057 Braga, Portugal

6. BioMark@ISEP/CEB—Center of Biological Engineering of Minho University, School of Engineering, Polytechnic Institute of Porto, 4249-015 Porto, Portugal

7. School of Health, Polytechnic of Porto, 4200-072 Porto, Portugal

8. Radiotherapy Service, São João Hospital Center, 4200-319 Porto, Portugal

9. Biomark@UC/CEB—Centre of Biological Engineering of Minho University, Department of Chemical Engineering, Faculty of Sciences and Technology, Coimbra University, 3030-790 Coimbra, Portugal

10. CINBIO, University of Vigo, 36310 Vigo, Spain

11. Southern Galicia Institute of Health Research (IISGS), and Biomedical Research Networking Center for Mental Health (CIBERSAM), 36310 Madrid, Spain

12. Institute of Molecular Pathology, Immunology of the University of Porto-IPATIMUP, 4200-465 Porto, Portugal

13. Department of Biomedicine, Biochemistry Unit, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal

14. Faculty of Health Sciences (FCS) & Hospital Escola Fernando Pessoa (HEFP), University Fernando Pessoa (UFP), 4249-004 Porto, Portugal

Abstract

More than 50% of all prostate cancer (PCa) patients are treated by radiotherapy (RT). Radioresistance and cancer recurrence are two consequences of the therapy and are related to dose heterogeneity and non-selectivity between normal and tumoral cells. Gold nanoparticles (AuNPs) could be used as potential radiosensitizers to overcome these therapeutic limitations of RT. This study assessed the biological interaction of different morphologies of AuNPs with ionizing radiation (IR) in PCa cells. To achieve that aim, three different amine-pegylated AuNPs were synthesized with distinct sizes and shapes (spherical, AuNPsp-PEG, star, AuNPst-PEG, and rods, AuNPr-PEG) and viability, injury and colony assays were used to analyze their biological effect on PCa cells (PC3, DU145, and LNCaP) when submitted to the accumulative fraction of RT. The combinatory effect of AuNPs with IR decreased cell viability and increased apoptosis compared to cells treated only with IR or untreated cells. Additionally, our results showed an increase in the sensitization enhancement ratio by cells treated with AuNPs and IR, and this effect is cell line dependent. Our findings support that the design of AuNPs modulated their cellular behavior and suggested that AuNPs could improve the RT efficacy in PCa cells.

Funder

Foundation for Science and Technology

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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