Drug intelligence / Profile preview

Pu27 Palmi

Development stage
Preclinical
Lead developer
University of Louisville
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
Administration
Parenteral
01

Overview

Pu27 Palmi is a palmitoylated (lipid-modified) G-quadruplex-forming oligonucleotide designed to target the c-MYC oncogene promoter. It is derived from the 27-nucleotide guanine-rich sequence (Pu27) located within the nuclease hypersensitive element (NHE) III1 of the c-MYC promoter region. By conjugating Pu27 with palmitic acid (palmitate), the oligonucleotide achieves enhanced G-quadruplex stability, improved cellular uptake, and reduced blood clearance compared to unmodified Pu27. Pu27 Palmi binds to the complementary C-rich strand of the NHEIII1 region, stabilizing the G-quadruplex structure and subsequently downregulating c-MYC transcription. This downregulation leads to decreased expression of c-MYC target genes (such as hTERT and VEGF), inhibiting cell proliferation and inducing apoptosis in cancer cells, particularly in triple-negative breast cancer (TNBC) and leukemia.

Other names
Pu27 palmitatePu-27 palmitatePu 27 palmitatelipid-modified Pu27palmitoyl-Pu27palmitoyl-Pu-27palmitoyl-Pu 27palmitoylated Pu27
02

Targets

MYC (MYC proto-oncogene protein)c-MYC promoter Pu27/NHEIII1 G-quadruplex-forming DNA

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