The collagen receptor
uPARAP
uPARAP is a collagen receptor which plays an important physiological role in collagen homeostasis by active internalization of collagen fragments. uPARAP displays highly efficient and constitutively active internalization and recycling properties
1
Extracellular collagen fibers are cleaved into smaller fragments by select matrix metalloproteases (MMPs)
2
Collagen fragments bind to endocytic receptor uPARAP on the cell surface
3
Collagen bound by uPARAP is actively endocytosed via clathrin-coated pits
4
uPARAP, and any bound collagen, is routed to early endosomes
5
uPARAP receptor is recycled to the cell surface for an additional internalization cycle
6
Collagen is further routed to lysosomes where is it broken down by proteases such as cathepsins
uPARAP displays a differentiated expression profile between healthy and cancer tissue, with several cancer types significantly overexpressing the receptor, including soft-tissue sarcoma, osteosarcoma, mesothelioma and glioblastoma multiforme (GBM).
Additionally, uPARAP is found to be upregulated by cells in the stromal compartment in multiple indications, including breast-, colon-, pancreas- and prostate cancers. uPARAP is a recycling endocytic receptor with extremely rapid internalization kinetics, providing highly efficient entry for ADCs targeting uPARAP-expressing cells
uPARAP
Expression on tumor cells
- Soft tissue sarcoma
- Osteosarcoma
- Mesothelioma
- Glioblastoma
Total copy number in tumor cells
10,000 – 100,000
Expression on healthy tissue
Limited uPARAP expression in healthy tissues and in activated fibroblasts/myfibroblasts of surrounding stroma in certain tissues
High Internalization rate
Target and bound ligand internalization
within 5-10 minutes
Receptor recycling upon ligand binding and internalization
Yes
Adcendo has generated in-vivo proof of concept data with our lead uPARAP ADC asset in multiple target indications and with multiple payload MoAs.