Drug intelligence / Profile preview

VASP shRNA

Development stage
Preclinical
Lead developer
University of Minnesota
Modality
Viral-delivered RNAi → In Vivo RNAi → Gene Silencing → Gene Therapies, RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intravenous
01

Overview

VASP shRNA is a gene-silencing therapeutic candidate designed to knock down the expression of vasodilator-stimulated phosphoprotein (VASP) via RNA interference. VASP is an actin-binding protein that promotes the β1-integrin-FAK-YAP1/TAZ signaling axis, a pathway critical for the colonization and growth of gastrointestinal (GI) cancer cells in the liver. By reducing VASP levels, this shRNA inhibits cancer cell attachment, migration, and proliferation in the liver parenchyma. Preclinical research conducted by institutions including the University of Minnesota and Mayo Clinic has demonstrated that VASP knockdown suppresses liver metastasis in mouse models of colorectal and pancreatic cancer, suggesting its potential as a therapeutic target for advanced GI malignancies.

Other names
vasodilator-stimulated phosphoprotein shRNAvasodilator-stimulated phosphoprotein short hairpin RNA
02

Targets

VASP (Vasodilator-stimulated phosphoprotein)

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