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Updated: Aug 2, 2025

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Current Medicinal Insights on Synthetic Small Molecules and Natural Origin Products as PD-1/PD-L1 Inhibitors
Shivanshu Pandey1, Balak Das Kurmi2, Preeti Patel1
1Department of Pharmaceutical Chemistry and Analysis, ISF College of Pharmacy, Moga, 142001, Punjab, India.
Abstract:
Cancer is one of the leading causes of death worldwide. Each year, millions of people are diagnosed with cancer; hence, researchers have always been curious and busy developing cancer treatments. Despite thousands of studies, cancer is still a major threat to human beings. One of the mechanisms through which cancer invades a human being is the immune escape mechanism, which has been the focus of studies in the past years. PD-1/PD-L1 pathway plays a major role in this immune escape. Therefore, research focusing on blocking this pathway has led to the discovery of molecules based on monoclonal antibodies that work quite well, but despite the successful application of monoclonal antibodies as inhibitors of the PD-1/PD-L1 pathway, there are some drawbacks, such as poor bioavailability and several immune-related adverse effects, which have led the researchers toward further investigation, thereby resulting in the discovery of different types of molecules, such as small molecule inhibitors, PROTAC-based molecules, and naturally derived peptide molecules that function as inhibitors of the PD-1/PD-L1 pathway. Here, in this review, we have summarized recent findings of these molecules and focused on their structural activity relationship. The development of these molecules has opened more prospects in cancer therapy.
Insights
Researchers are exploring novel small molecules, PROTACs, and peptides to inhibit the PD-1/PD-L1 pathway, offering new cancer immunotherapy strategies beyond monoclonal antibodies.
Area of Science:
- Oncology
- Immunology
- Medicinal Chemistry
Background:
- Cancer remains a leading global cause of death, with immune evasion being a critical challenge.
- The programmed cell death protein 1 (PD-1)/programmed death-ligand 1 (PD-L1) pathway is a key mechanism for cancer immune escape.
- Monoclonal antibodies targeting PD-1/PD-L1 have shown efficacy but have limitations including poor bioavailability and adverse effects.
Conclusions:
- Novel small molecule, PROTAC, and peptide inhibitors offer promising alternatives for targeting the PD-1/PD-L1 pathway in cancer therapy.
- These agents may provide improved bioavailability and reduced adverse effects compared to monoclonal antibodies.
- Further research into these molecules holds significant potential for advancing cancer treatment strategies.
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