Department of Physics and Astronomy, University of Victoria, Victoria, BC V8P 5C2, Canada.
Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC V8P 5C2, Canada.
Int J Mol Sci. 2023 Aug 7;24(15):12523. doi: 10.3390/ijms241512523.
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% ( < 0.05) increase in proliferation and a 13.0% ( < 0.05) decrease in DNA DSB when compared to monoculture samples, However, they displayed a 175% ( < 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% ( < 0.05) in spheroid size and an increase of 14.3% ( < 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.
胰腺癌是最致命的癌症之一,现有的治疗方法效果不佳。迫切需要新的、更有效的治疗方法来应对这一重大医学挑战。在这项研究中,我们旨在评估金纳米颗粒(GNPs)与放射治疗(RT)联合的抗癌疗效。使用 MIA PaCa-2 癌细胞和患者来源的癌相关成纤维细胞(CAF-98)的 3D 胰腺癌共培养球体模型。用 GNPs(7.5 μg/mL)和 2 Gy RT 处理球体。通过 CellTiter-Glo 3D 测定法评估球体的细胞活力,并通过表达 DNA 损伤标志物 53BP1 评估免疫荧光测定法的 DNA DSB。与单核培养物相比,共培养物样本的增殖增加了 10.8%(<0.05),DNA DSB 减少了 13.0%(<0.05),然而,与单核培养物球体相比,它们的 GNPs 摄取量增加了 175%(<0.001)。使用 GNPs/RT,我们能够显示出显著的减少 6.2%(<0.05)的球体大小和增加 14.3%(<0.05)的 DNA DSB 损伤在共培养物样本中。GNPs 与 RT 的联合具有显著的放射增敏作用,代表了一种增强癌症治疗效果的有前途的方法。这些作用在更具治疗抗性的共培养球体模型中尤为显著。