Oncology Research

PNC-27

Targeted anti-cancer peptide (p53-derived) causing tumor necrosis

Overview

PNC-27 is a synthetic peptide containing the p53 binding domain (residues 12-26) fused to a transmembrane-penetrating sequence. It is engineered to selectively kill cancer cells by targeting HDM-2 proteins abnormally expressed on their membranes. Upon binding, it creates pores that destroy the tumor cell (necrosis) while leaving healthy cells unharmed. It is effective even in cancers with mutant p53.

Chemical Information

IUPAC Name
p53(12-26)-Transmembrane Domain Fusion
Sequence
Pro-Pro-Leu-Ser-Gln-Etc (Fusion Sequence)
Molecular Mass
4031.7 Da
Formula
C188H293N53O54S2
Chemical Structure not available

Mechanism of Action

Functions as a membranolytic agent that exploits a specific vulnerability in cancer cells: the presence of HDM-2 on the cell membrane. In normal cells, HDM-2 is nuclear; in cancer cells, it is often overexpressed and found on the surface. PNC-27 binds to this membrane-bound HDM-2 via its p53 leader sequence. Upon binding, the peptide undergoes a conformational change, assembling into transmembrane pores (holes). This breaches the cell membrane, causing an influx of ions and water that leads to rapid necrosis (cell bursting). Because normal cells lack membrane-bound HDM-2, they remain completely unaffected. Crucially, this mechanism is p53-independent, meaning it kills tumors even if their p53 gene is mutated or absent.

Potential Research Fields

Solid Tumors (Breast, Colon, Pancreatic)LeukemiaChemo-resistanceMembrane Biology

Recent Research

Research confirms PNC-27 as a highly selective 'necrotic agent.' Unlike chemotherapy which induces apoptosis (programmed cell death) and can fail if the apoptosis genes (like p53) are broken, PNC-27 acts physically to punch holes in the cancer cell. Recent studies highlight its efficacy across a broad spectrum—from solid tumors like pancreatic and ovarian cancer to liquid tumors like leukemia. Current investigations focus on its safety profile, repeatedly showing that it spares healthy bone marrow and epithelial cells, making it a promising candidate for targeted therapy with minimal systemic side effects.

Bibliography / Scientific References

Related Peptides

No related peptides found.

Peptide Information Guide
Administration Type
Injectable (Subcutaneous/Tumoral)

Injectable administration protocol for research.

Vial Strength
10mg
Reconstitution
Reconstitute with 2ml bacteriostatic water
Dosage Options
1 mg (20 units)
Daily
Protocol for 10mg vial reconstituted w/ 2ml water
Schedule
1x daily
Timing: One specific day.
Duration
6 Weeks
Potential Side Effects
Injection site inflammation
moderatecommon
Research Use Only

This information is for research purposes only. Always consult with a healthcare professional before starting any peptide protocol. Individual responses may vary, and proper medical supervision is recommended for all peptide therapies.