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VEGF-siRNA lentivirus refers to a gene therapy approach that utilizes a lentiviral vector to deliver small interfering RNA (siRNA) or short hairpin RNA (shRNA) molecules. These RNA molecules are designed to specifically target and silence the expression of Vascular Endothelial Growth Factor (VEGF) through RNA interference (RNAi). By reducing VEGF protein levels, this therapeutic strategy aims to inhibit angiogenesis (the formation of new blood vessels), thereby suppressing tumor growth and metastasis in various cancers, and preventing neovascularization in ocular pathologies. This approach is primarily in the research and pre-clinical stages of development.
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