| Literature DB >> 33918146 |
Darya Javadrashid1, Amir Baghbanzadeh1, Afshin Derakhshani1,2, Patrizia Leone3, Nicola Silvestris2,4, Vito Racanelli3, Antonio Giovanni Solimando2,3, Behzad Baradaran1,5.
Abstract
Genetic alterations, especially the K-Ras mutation, carry the heaviest burden in the progression of pancreatic precursor lesions into pancreatic ductal adenocarcinoma (PDAC). The tumor microenvironment is one of the challenges that hinder the therapeutic approaches from functioning sufficiently and leads to the immune evasion of pancreatic malignant cells. Mastering the mechanisms of these two hallmarks of PDAC can help us in dealing with the obstacles in the way of treatment. In this review, we have analyzed the signaling pathways involved in PDAC development and the immune system's role in pancreatic cancer and immune checkpoint inhibition as next-generation therapeutic strategy. The direct targeting of the involved signaling molecules and the immune checkpoint molecules, along with a combination with conventional therapies, have reached the most promising results in pancreatic cancer treatment.Entities:
Keywords: PDAC; gene mutation; immune checkpoint; pancreatic adenocarcinoma; pancreatic cancer; signaling pathway
Year: 2021 PMID: 33918146 DOI: 10.3390/biomedicines9040373
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059