Students Summer in Oncology at Anderson Research (SOAR)
 

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Description

This study evaluated the efficacy of liposomal nanoparticles (LNPs) in delivering Wnt/β-catenin-inhibiting mIR-124 plasmids to melanomas. In vitro, LNPs with mIR-124 were applied to B16N2 melanoma cells. In vivo, LNPs were injected into B16N2 tumors in mice. Delivery success was confirmed via flow cytometry and RT-PCR, assessing GFP expression, tumor transition markers, and Wnt/β-catenin signaling. Overall, the findings suggested that LNP-mediated delivery of Wnt/β-catenin inhibitors holds promise as a therapeutic strategy for melanoma, with trends indicating a reversal of epithelial-mesenchymal transition (EMT) and slowed melanoma progression.

Program Affiliation

SOAR

DOI

https://doi.org/10.52519/00157

Publication Date

2024

Keywords

Melanoma, Liposomal Nanoparticles (LNPs), Wnt/β-catenin Pathway, mIR-124

Liposomal Nanoparticle Mediated Gene Modulation for the Treatment of Melanoma in the Murine Model

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