Drug intelligence / Profile preview

P2Y1 shRNA

Development stage
Preclinical
Lead developer
NYU Langone Health
Modality
Viral-delivered RNAi → In Vivo RNAi → Gene Silencing → Gene Therapies, RNA Therapeutics → Nucleic Acid Therapeutics
01

Overview

P2Y1 shRNA is a gene-silencing therapeutic candidate designed to knock down the expression of the P2Y1 purinergic receptor (P2RY1). In glioblastoma (GBM) research, it is utilized to investigate and inhibit the purinergic signaling pathway driven by extracellular ATP and ADP. By reducing P2Y1 levels, this short hairpin RNA (shRNA) inhibits tumor cell-autonomous calcium oscillations, which are critical for GBM growth, sphere formation, and invasion. Preclinical studies using patient-derived glioblastoma cells have demonstrated that P2Y1 knockdown significantly reduces both spontaneous and ligand-induced calcium waves, suggesting that targeting this Gq protein-coupled receptor via RNA interference could be a viable strategy to limit tumor progression in aggressive brain malignancies.

Other names
shRNA knockdown of P2Y1P2RY1 shRNAP-2RY1 shRNAP 2RY1 shRNA
02

Targets

IFIH1 (MDA5)EIF2AK2 (Interferon-induced protein kinase R)TLR3 (Toll-like receptor 3)P2RY1 (Purinergic Receptor P2Y1)DICER1 (Dicer ribonuclease III)TLR7/8 (Toll-like receptor 7 and Toll-like receptor 8)AGO2 (Argonaute RISC catalytic component 2)

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