Drug intelligence / Profile preview

vegf-siRNA lentivirus

Development stage
Preclinical
Lead developer
Renji Hospital
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Gene Editing → Gene Therapies, Gene Silencing → Gene Therapies, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Lentiviral Vectors → Retroviral Vectors → Viral Vectors → Gene Addition/Replacement → Gene Therapies
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Overview

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.

Other names
Lentivirus-mediated VEGF-C siRNALentivirus-mediated siRNA targeting VEGFVEGF-shRNA lentivirus
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Targets

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