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Effect of fractalkine-Fc delivery in experimental lung metastasis using DNA/704 nanospheres
P Richard-Fiardo1, B Cambien, E Pradelli
1Archet I, Nice, France.
Abstract:
The lung is one target organ to which solid tumors frequently metastasize. Given the systemic adverse effects of currently available treatments, developing effective strategies of drug/gene delivery directly to the lungs is therefore needed. Aerosol delivery is a non-invasive gene transfer approach to target the airways. Here, we sought to evaluate the potential to deliver a fractalkine (FKN)-encoding plasmid formulated with the tetrafunctional amphiphilic block copolymer 704 through aerosolization in two models of pulmonary metastases. FKN is a chemokine recently described as a good candidate to stimulate a strong antitumor immune response in various forms of cancers. Here, we have assessed the effect of single and repeated aerosolizations of FKN-encoding plasmid formulated with 704 on the development of experimental lung metastases of mouse colon carcinoma and osteosarcoma. For this purpose, we have designed FKN-Fc sequences encoding an optimized version of the chemokine. Repeated intratracheal administrations of 704/FKN-Fc markedly inhibited growth of experimental lung metastases of CT-26 and K7M2 cells. Our results showed that tetrafunctional amphiphilic block copolymer 704 is a highly efficient synthetic vector for mediating local and safe gene transfer into the lung. In addition, FKN-Fc gene therapy of pulmonary nodules may provide a promising immunotherapeutic approach.
Insights
Aerosol delivery of a fractalkine (FKN)-encoding plasmid using copolymer 704 effectively inhibited lung metastases in mouse models. This non-invasive gene therapy shows promise for treating pulmonary tumors and stimulating antitumor immunity.
Area of Science:
- Oncology
- Gene Therapy
- Nanotechnology
Background:
- The lung is a common site for solid tumor metastasis.
- Current systemic treatments for lung metastases have significant adverse effects.
- Targeted, non-invasive drug/gene delivery to the lungs is needed.
Purpose of the Study:
- To evaluate aerosol delivery of a fractalkine (FKN)-encoding plasmid formulated with tetrafunctional amphiphilic block copolymer 704.
- To assess the efficacy of this approach in preclinical models of pulmonary metastases.
Main Methods:
- Aerosolization of FKN-encoding plasmid formulated with copolymer 704.
- Intratracheal administration in mouse models of colon carcinoma (CT-26) and osteosarcoma (K7M2) lung metastases.
- Assessment of tumor growth inhibition following single and repeated administrations.
Main Results:
- Repeated intratracheal administration of 704/FKN-Fc significantly inhibited the growth of experimental lung metastases in both CT-26 and K7M2 models.
- Copolymer 704 demonstrated efficient and safe gene transfer to the lung via aerosolization.
- FKN-Fc gene therapy showed potential for treating pulmonary metastases.
Conclusions:
- Aerosolized FKN-Fc gene therapy using copolymer 704 is a promising strategy for managing lung metastases.
- This approach offers a non-invasive, targeted method for gene delivery to the lungs.
- FKN-Fc gene therapy may represent a novel immunotherapeutic approach for pulmonary tumors.
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