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FGFR2 shRNA

Development stage
Preclinical
Lead developer
Nippon Medical School
Modality
Viral-delivered RNAi → In Vivo RNAi → Gene Silencing → Gene Therapies, RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intraperitoneal
01

Overview

FGFR2 shRNA is a short hairpin RNA-based therapeutic candidate designed to silence the expression of fibroblast growth factor receptor 2 (FGFR2). It specifically targets the common exon of the FGFR2 IIIb and IIIc isoforms, which are frequently overexpressed in pancreatic ductal adenocarcinoma (PDAC). By inducing RNA interference (RNAi), the shRNA reduces FGFR2 mRNA and protein levels, leading to the inhibition of downstream MAPK/ERK signaling pathways. This suppression results in decreased cancer cell proliferation and reduced expression of vascular endothelial growth factor A (VEGF-A), thereby inhibiting angiogenesis. Research conducted at Nippon Medical School has demonstrated its efficacy in reducing tumor growth in preclinical models of pancreatic cancer.

Other names
FGFR2 short hairpin RNAFGFR-2 short hairpin RNAFGFR 2 short hairpin RNAFGFR2-shRNAFGFR-2-shRNAFGFR 2-shRNA
02

Targets

FGFR2 (Keratinocyte growth factor receptor)

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