Drug intelligence / Profile preview

PPRH2

Development stage
Preclinical
Lead developer
University of Barcelona
Modality
MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Gene Therapies
Administration
Intravenous, Intratumoral
01

Overview

PPRH2 (specifically HpKras-P2) is a polypurine reverse Hoogsteen hairpin (PPRH) oligonucleotide designed to target the KRAS oncogene. Developed by researchers at the University of Barcelona, PPRHs are a novel class of gene-silencing agents consisting of two polypurine domains linked by a thymidine loop. These molecules bind to specific polypyrimidine tracks in the genomic DNA—typically within the promoter region—through Hoogsteen base pairing, forming a stable triplex structure that displaces the fourth DNA strand and inhibits transcription. PPRH2 specifically targets the KRAS promoter to downregulate its expression. In preclinical studies, particularly in ovarian and lung cancer models, PPRH2 has demonstrated the ability to inhibit cell proliferation, reduce 3D spheroid growth, and significantly enhance the efficacy of chemotherapeutic agents such as cisplatin and paclitaxel by overcoming chemoresistance associated with KRAS overexpression.

Other names
KRAS-targeting PPRHpolypurine reverse Hoogsteen hairpin 2HpKras-P2 oligonucleotideHpKras-P-2 oligonucleotideHpKras-P 2 oligonucleotide
02

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