Drug intelligence / Profile preview

HOP230-245

Development stage
Preclinical
Lead developer
Northwestern University
Modality
Peptides
Administration
Intratumoral
01

Overview

HOP230-245 is a synthetic peptide therapeutic designed to disrupt the interaction between the cellular prion protein (PrPC) and the heat shock organizing protein (HOP, also known as STIP1). This interaction is a critical driver of self-renewal, proliferation, and therapy resistance in glioblastoma stem cells (GSCs). By binding to the 106-126 amino acid domain of PrPC, the peptide competitively inhibits the binding of HOP and other ligands, thereby suppressing downstream signaling pathways that promote tumorigenesis and hypoxia-induced resistance. Preclinical research indicates that HOP230-245 can sensitize GSCs to the alkylating agent temozolomide (TMZ) and inhibit glioblastoma growth in vivo, suggesting its potential as a combination therapy for aggressive brain tumors.

Other names
HOP peptideHOP(230-245)
02

Targets

PRNP (Cellular Prion Protein)

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