NANOPARTICLE-MEDIATED TUMOR CELL EXPRESSION OF MIL-12 VIA SYSTEMIC GENE DELIVERY TREATS SYNGENEIC MODELS OF MURINE LUNG CANCERS

Nanoparticle-mediated tumor cell expression of mIL-12 via systemic gene delivery treats syngeneic models of murine lung cancers

Nanoparticle-mediated tumor cell expression of mIL-12 via systemic gene delivery treats syngeneic models of murine lung cancers

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Abstract Treatment of cancers in the lung remains a critical challenge in the Body Cream clinic for which gene therapy could offer valuable options.We describe an effective approach through systemic injection of engineered polymer/DNA nanoparticles that mediate tumor-specific expression of a therapeutic gene, under the control of the cancer-selective progression elevated gene 3 (PEG-3) promoter, to treat tumors in the lungs of diseased mice.A clinically tested, untargeted, polyethylenimine copyright was selected to aid rapid transition to clinical studies, and a CpG-free plasmid backbone and coding sequences were used to reduce inflammation.

Intravenous administration of nanoparticles expressing murine single-chain interleukin 12, under the control of PEG-3 promoter, significantly improved the survival of mice in both an orthotopic and a metastatic model of lung cancer with Over the Range Microwave no marked symptoms of systemic toxicity.These outcomes achieved using clinically relevant nanoparticle components raises the promise of translation to human therapy.

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