Development of a targeted delivery platform for checkpoint inhibitors

NIH RePORTER · NIH · R01 · $354,563 · view on reporter.nih.gov ↗

Abstract

Abstract The goal of this proposed research is to develop a targeted delivery platform for checkpoint inhibitors. The platform will contain a targeting ligand, an enzyme-responsive linker, and a peptide- based checkpoint inhibitor. We recently discovered several peptide-based PD-L1 inhibitors that can be potentially used for cancer immunotherapy. In this study, we will evaluate the platform in an advanced prostate cancer model. Particularly, we propose to link a PSMA-specific ligand to the anti-PD-L1 peptides via a PSA-cleavable linker. The overall objectives of this project are: 1) to develop a targeted anti-PD-L1 peptide for cancer immunotherapy; 2) to evaluate its therapeutic effect using humanized mice implanted with human castration-resistant prostate cancer (CRPC) cells. The long-term goal of the project is to develop a targeted peptide-based platform for cancer immunotherapy. Our central hypothesis is that cancer growth and metastasis can be effectively inhibited by targeted delivery of anti-PD-L1 peptides to cancer cells. At the completion of this project, we expect to pave the way for the future development of a targeted PD-L1 inhibitor for cancer immunotherapy. Successful completion of the proposed studies is also expected to provide a peptide-based platform (by changing the targeting ligand and the tissue-specific linker) for other peptide-based checkpoint inhibitors.

Key facts

NIH application ID
10250482
Project number
5R01CA231099-04
Recipient
UNIVERSITY OF MISSOURI KANSAS CITY
Principal Investigator
Kun Cheng
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$354,563
Award type
5
Project period
2018-09-01 → 2023-08-31