Adenosine, Schizophrenia and Cancer: Does the Purinergic System Offer a Pathway to Treatment?

Int J Mol Sci. 2022 Oct 5;23(19):11835. doi: 10.3390/ijms231911835.

Abstract

For over a century, a complex relationship between schizophrenia diagnosis and development of many cancers has been observed. Findings from epidemiological studies are mixed, with reports of increased, reduced, or no difference in cancer incidence in schizophrenia patients. However, as risk factors for cancer, including elevated smoking rates and substance abuse, are commonly associated with this patient population, it is surprising that cancer incidence is not higher. Various factors may account for the proposed reduction in cancer incidence rates including pathophysiological changes associated with disease. Perturbations of the adenosine system are hypothesized to contribute to the neurobiology of schizophrenia. Conversely, hyperfunction of the adenosine system is found in the tumor microenvironment in cancer and targeting the adenosine system therapeutically is a promising area of research in this disease. We outline the current biochemical and pharmacological evidence for hypofunction of the adenosine system in schizophrenia, and the role of increased adenosine metabolism in the tumor microenvironment. In the context of the relatively limited literature on this patient population, we discuss whether hypofunction of this system in schizophrenia, may counteract the immunosuppressive role of adenosine in the tumor microenvironment. We also highlight the importance of studies examining the adenosine system in this subset of patients for the potential insight they may offer into these complex disorders.

Keywords: adenosine; cancer; epidemiology; purinergic signaling; schizophrenia.

Publication types

  • Review

MeSH terms

  • Adenosine / metabolism
  • Humans
  • Incidence
  • Neoplasms*
  • Schizophrenia* / drug therapy
  • Schizophrenia* / metabolism
  • Tumor Microenvironment

Substances

  • Adenosine

Grants and funding

This work was supported by RO1 MH107487 and MH121102 (REM). This project was supported by Grant YIG-1-139-20 awarded to SMOD from the American Foundation for Suicide Prevention. The content is solely the responsibility of the authors and does not necessarily represent the official views of the American Foundation for Suicide Prevention.