Affiliations 

  • 1 Division of Pharmacology and Toxicology, Guru Nanak Institute of Pharmaceutical Science and Technology (Autonomous), Affiliated to Maulana Abul Kalam Azad University of Technology, West Bengal, 157/F, Nilgunj Road, Panihati, Sodepur, Kolkata, 700114, India
  • 2 Department of Pharmaceutical Technology, Jadavpur University, Kolkata, 700032, West Bengal, India
  • 3 Faculty of Pharmacy, MAHSA University, Bandar Saujana Putra, Jenjarom, 42610, Selangor, Malaysia
  • 4 Division of Life Sciences, Institute of Advanced Study in Science and Technology (IASST), An Autonomous Institute under Department of Science & Technology, Govt. of India, Vigyan Path, Guwahati, 781035, Assam, India
PMID: 36788687 DOI: 10.2174/1871530323666230213121803

Abstract

Programmed cell death protein 1 or Programmed death-1 (PD-1) and Programmed Cell Death Ligand 1 (PD-L1) research have tremendously been taken into great consideration in the field of cancer immune pharmacology. Cancer immunotherapy has been convoyed by a capable outcome over the past few years. PD-1 and PD-L1 play a pivotal role in attenuating immune involvement, modulating the activity of T-cells, and promoting different types of programmed cell death. Participation of antigen-specific T cells and regulatory T cells and their acute mutations during cancer cell invasion and migration may lead to challenges for three programmed cell death methods, namely, pyroptosis, apoptosis, and necroptosis called "PANoptosis". This review aimed to explore the correlation between the PD-1/PD-L1 pathway in "PANoptosis" using available recently published literature with several schematic representations. Hopefully, the review will facilitate the biomedical scientist targeting cancer immune pharmacological aspect for the management of Breast Adenocarcinoma shortly.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.