| Literature DB >> 27247189 |
Aeju Lee1, Daniele Di Mascolo1, Marco Francardi1, Federica Piccardi1, Tiziano Bandiera1, Paolo Decuzzi2.
Abstract
Nanoparticles can simultaneously deliver multiple agents to cancerous lesions enabling de facto combination therapies. Here, spherical polymeric nanoconstructs (SPNs) are loaded with anti-cancer - docetaxel (DTXL) - and anti-inflammatory - diclofenac (DICL) - molecules. In vitro, combination SPNs kill U87-MG cells twice as efficiently as DTXL SPNs, achieving a IC50 of 90.5nM at 72h. Isobologram analysis confirms a significant synergy (CI=0.56) between DTXL and DICL. In mice bearing non-orthotopic glioblastoma multiforme tumors, combination SPNs demonstrate higher inhibition in disease progression. At 70days post treatment, the survival rate of mice treated with combination SPNs is of about 70%, against a 40% for DTXL SPNs and 0% for free DTXL. Combination SPNs dramatically inhibit COX-2 expression, modulating the local inflammatory status, and increase Caspase-3 expression, which is directly related to cell death. These results suggest that the combination of anti-cancer and anti-inflammatory molecules constitutes a potent strategy for inhibiting tumor growth.Entities:
Keywords: Cancer inflammation; Combinatorial therapy; Nanoparticles; Tumor microenvironment
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Year: 2016 PMID: 27247189 DOI: 10.1016/j.nano.2016.05.012
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307