结缔组织增生
纳米医学
癌症研究
光动力疗法
医学
细胞外基质
程序性细胞死亡
启动(农业)
癌症
化学
纳米颗粒
纳米技术
细胞凋亡
内科学
材料科学
生物
生物化学
有机化学
植物
胰腺癌
发芽
作者
Marta Overchuk,Kara M. Harmatys,Shrey Sindhwani,Maneesha A. Rajora,Adam Koebel,Danielle M. Charron,Abdullah M. Syed,Juan Chen,Martin G. Pomper,Brian C. Wilson,Warren C. W. Chan,Gang Zheng
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-12-10
卷期号:21 (1): 344-352
被引量:49
标识
DOI:10.1021/acs.nanolett.0c03731
摘要
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.
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