PD-1/PD-L1 AXIS INHIBITORS AS PROMISING STRATEGY FOR MANAGEMENT OF HEPATOCELLULAR CARCINOMA: EXPECTATIONS, BOUNDARIES AND PITFALLS | ||||
Journal of the Medical Research Institute | ||||
Article 1, Volume 44, Issue 2, December 2023, Page 1-8 PDF (415.12 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/jmalexu.2023.323222 | ||||
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Authors | ||||
Yousra Y. El Banna* 1; Raghda Abo Ayana2; Magda Nasr2; Maged W. Helmy3 | ||||
1Department of Pharmacology and Toxicology, Clinical and Biological Sciences Division, College of Pharmacy, Arab Academy for Science, Technology and Maritime Transport, Alexandria, Egypt | ||||
2Department of Pharmacology and Experimental Therapeutics, Medical Research Institute, Alexandria University, Alexandria, Egypt | ||||
3Pharmacology and Toxicology, Faculty of Pharmacy, Damanhour University, Egypt | ||||
Abstract | ||||
Hepatocellular carcinoma (HCC), the most prevalent primary liver cancer and a leading cause of cancer-related deaths worldwide, has prompted exploration into innovative treatment avenues. Notably, cancer immunotherapy has emerged as a promising strategy, with immune checkpoint inhibitors, specifically targeting the programmed cell death 1 (PD-1) and its ligand (PD-L1), revolutionizing cancer care. PD-1 is a crucial protein in suppressing immune responses and promoting self-tolerance by regulating T-cell function. The PD-1/PD-L1 axis is responsible for immune evasion in cancer cells making it a focal point in cancer therapy. However, despite the potential of PD-1/PD-L1 inhibitors, their clinical utility is hampered by significant immune-related adverse effects. This underscores the urgency to develop novel inhibitors, including small molecules and peptides that target the PD-1/PD-L1 axis to better meet clinical demands. This review focuses on elucidating the biological mechanisms of PD-1/PD-L1 immune checkpoints and their role in both the healthy immune system and the tumor microenvironment. Limitations to this treatment approach include low response rates in certain cancers, immune-related toxicity, and the development of drug resistance. Overcoming these limitations is crucial to expand the use of PD-1/PD-L1 blockade in cancer treatment and improve response rates and survival times for cancer patients | ||||
Keywords | ||||
HCC; cancer immunotherapy; immune checkpoints; PD1-PD-L1 axis; PD-L1 inhibitor | ||||
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