Drug intelligence / Profile preview

G-NP

Development stage
Preclinical
Lead developer
Huazhong University of Science and Technology
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

G-NP is an experimental nanoparticle-based RNA interference (RNAi) therapeutic designed to silence the expression of growth-regulated oncogene alpha (Gro-α), also known as CXCL1. Gro-α is a pro-inflammatory chemokine and oncogene that promotes tumor cell proliferation, migration, and angiogenesis, particularly in ovarian clear cell carcinoma. The G-NP formulation consists of siRNA molecules encapsulated within a nanoparticle carrier, which protects the genetic material from degradation and facilitates cellular uptake. In many research applications, the nanoparticle is further modified with a follicle-stimulating hormone (FSH) peptide (specifically FSH β 33-53) to target the follicle-stimulating hormone receptor (FSHR), which is highly expressed in ovarian cancer tissues. This targeted approach (often referred to as FSH-G-NP) aims to improve the delivery of the siRNA payload to malignant cells while reducing systemic toxicity. Preclinical studies have demonstrated that G-NP-mediated silencing of Gro-α can significantly inhibit tumor growth and enhance the sensitivity of cancer cells to other treatments.

Other names
Gro-alpha siRNA nanoparticleCXCL1 siRNA nanoparticleCXCL-1 siRNA nanoparticleCXCL 1 siRNA nanoparticleFSH-G-NP
02

Targets

CXCL1 (C-X-C motif chemokine ligand 1)Follicle-stimulating hormone receptor messenger RNA (FSHR mRNA)

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