The potential role of purinergic signaling in cancer therapy: perspectives on anti-CD73 strategies for prostate cancer.

Front Immunol

Escola de Medicina, Programa de Pós-Graduação em Medicina e Ciências da Saúde, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil.

Published: October 2024

AI Article Synopsis

  • Purines and pyrimidines are key signaling molecules in tumors that influence the immune response against cancer, with purinergic signaling pathways significantly impacting cancer development and progression.
  • CD39 and CD73, enzymes that convert ATP and ADP into adenosine, contribute to immunosuppression in various cancers, making them potential targets for immunotherapy.
  • This review focuses on the critical role of the adenosine/CD73 pathway in prostate cancer treatment, advocating for anti-CD73 as a promising pharmacological strategy to improve patient outcomes.

Article Abstract

Purines and pyrimidines are signaling molecules in the tumor microenvironment that affect cancer immunity. The purinergic signaling pathways have been shown to play an important role in the development and progression of cancer. CD39 and CD73 are ectonucleotidases responsible for breaking down ATP or ADP into adenosine, which regulates immunosuppression in various types of cancer. These enzymes have been studied as a potential therapeutic target in immunotherapy, and recent research suggests a correlation between ectonucleotidases and clinical outcomes in cancer.Prostate cancer is the most diagnosed cancer in men, after non-melanoma skin tumors, and is the second leading cause of death in men in the world. Despite having long survival periods, patients often receive excessive or insufficient treatment. Within this complex landscape, the adenosine/CD73 pathway plays a crucial role. Therefore, this review aims to highlight new findings on the potential role of purinergic signaling in cancer treatment and emphasizes the importance of anti-CD73 as a pharmacological strategy for prostate cancer therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11442216PMC
http://dx.doi.org/10.3389/fimmu.2024.1455469DOI Listing

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