Princess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, Ontario M5G 1L7, Canada.
Institute of Biomedical Engineering, University of Toronto, Toronto, Ontario M5G 1L7, Canada.
Nano Lett. 2021 Jan 13;21(1):344-352. doi: 10.1021/acs.nanolett.0c03731. Epub 2020 Dec 10.
Limited tumor nanoparticle accumulation remains one of the main challenges in cancer nanomedicine. Here, we demonstrate that subtherapeutic photodynamic priming (PDP) enhances the accumulation of nanoparticles in subcutaneous murine prostate tumors ∼3-5-times without inducing cell death, vascular destruction, or tumor growth delay. We also found that PDP resulted in an ∼2-times decrease in tumor collagen content as well as a significant reduction of extracellular matrix density in the subendothelial zone. Enhanced nanoparticle accumulation combined with the reduced extravascular barriers improved therapeutic efficacy in the absence of off-target toxicity, wherein 5 mg/kg of Doxil with PDP was equally effective in delaying tumor growth as 15 mg/kg of Doxil. Overall, this study demonstrates the potential of PDP to enhance tumor nanomedicine accumulation and alleviate tumor desmoplasia without causing cell death or vascular destruction, highlighting the utility of PDP as a minimally invasive priming strategy that can improve therapeutic outcomes in desmoplastic tumors.
肿瘤纳米颗粒的积累有限仍然是癌症纳米医学的主要挑战之一。在这里,我们证明亚治疗光动力预处理 (PDP) 可以在不诱导细胞死亡、血管破坏或肿瘤生长延迟的情况下,将皮下鼠前列腺肿瘤中的纳米颗粒积累增加约 3-5 倍。我们还发现,PDP 导致肿瘤胶原含量减少约 2 倍,以及 subendothelial 区细胞外基质密度显著降低。增强的纳米颗粒积累结合减少的血管外屏障,在没有脱靶毒性的情况下提高了治疗效果,其中 PDP 联合 5mg/kg 的 Doxil 的疗效与 15mg/kg 的 Doxil 相当,可以延缓肿瘤生长。总的来说,这项研究表明 PDP 具有增强肿瘤纳米医学积累和减轻肿瘤纤维变性的潜力,而不会导致细胞死亡或血管破坏,突出了 PDP 作为一种微创预处理策略的实用性,可改善纤维变性肿瘤的治疗效果。