Utilizing Gold Nanoparticles as Prospective Radiosensitizers in 3D Radioresistant Pancreatic Co-Culture Model

Author:

Alhussan Abdulaziz1ORCID,Jackson Nolan1,Calisin Reinali1,Morgan Jessica23,Beckham Wayne14,Chithrani Devika B.14567ORCID

Affiliation:

1. Department of Physics and Astronomy, University of Victoria, Victoria, BC V8P 5C2, Canada

2. Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC V8P 5C2, Canada

3. Trev and Joyce Deeley Research Centre, British Columbia Cancer-Victoria, Victoria, BC V8R 6V5, Canada

4. Radiation Oncology, British Columbia Cancer-Victoria, Victoria, BC V8R 6V5, Canada

5. Centre for Advanced Materials and Related Technologies, Department of Chemistry, University of Victoria, Victoria, BC V8P 5C2, Canada

6. Department of Medical Sciences, University of Victoria, Victoria, BC V8P 5C2, Canada

7. Department of Computer Science, Mathematics, Physics and Statistics, Okanagan Campus, University of British Columbia, Kelowna, BC V1V 1V7, Canada

Abstract

Pancreatic cancer stands among the deadliest forms of cancer, and the existing treatments fall short of providing adequate efficacy. Novel and more effective treatment approaches are urgently required to address this critical medical challenge. In this study, we aimed to evaluate the anti-cancer efficacy of gold nanoparticles (GNPs) in combination with radiotherapy (RT). A 3D pancreatic cancer co-culture spheroid model of MIA PaCa-2 cancer cells and patient-derived cancer-associated fibroblasts (CAF-98) was used. The spheroids were treated with GNPs (7.5 μg/mL) and 2 Gy of RT. The spheroids’ cell viability was assessed through the CellTiter-Glo 3D assay, and an immunofluorescence assay was used to assess the DNA DSBs via the expression of the DNA damage marker 53BP1. Co-culture samples showed a 10.8% (p < 0.05) increase in proliferation and a 13.0% (p < 0.05) decrease in DNA DSB when compared to monoculture samples, However, they displayed a 175% (p < 0.001) increase in GNPs uptake when compared to monoculture spheroids. Using GNPs/RT, we were able to show a significant reduction of 6.2% (p < 0.05) in spheroid size and an increase of 14.3% (p < 0.05) in DNA DSB damage in co-culture samples. The combination of GNPs with RT demonstrated remarkable radiosensitization effects, representing a promising approach to enhance cancer treatment efficacy. These effects were particularly noteworthy in the more treatment-resistant co-culture spheroid model.

Funder

Kuwait Foundation for the Advancement of Sciences

NanoMedicines Innovation Network Strategic Initiative fund

John R. Evans Leaders Fund

British Columbia Knowledge Development Fund

Natural Sciences and Engineering Research Council of Canada

University of Victoria

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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