| Literature DB >> 33301689 |
Marta Overchuk1,2, Kara M Harmatys1, Shrey Sindhwani2, Maneesha A Rajora1,2, Adam Koebel3, Danielle M Charron1,2, Abdullah M Syed4, Juan Chen1, Martin G Pomper5, Brian C Wilson1,6, Warren C W Chan2, Gang Zheng1,2,6.
Abstract
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.Entities:
Keywords: PSMA; extracellular matrix; nanomedicine; photodynamic therapy; prostate cancer
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Year: 2020 PMID: 33301689 DOI: 10.1021/acs.nanolett.0c03731
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189