Renin-angiotensin system and cancer: epidemiology, cell signaling, genetics and epigenetics

Clin Transl Oncol. 2021 Apr;23(4):682-696. doi: 10.1007/s12094-020-02488-3. Epub 2020 Sep 15.

Abstract

Day by day, the health and economical burden of cancer increases globally. Indeed it can be considered that there is ''cancer pandemic''. Blocking the renin-angiotensin system (RAS) by angiotensin-converting enzyme (ACE) inhibitors (ACEI) or angiotensin-receptor blockers (ARB) are widely used measures to treat hypertension and heart failure. It has been recently suggested the activation and blocking of RAS has been associated with various types of cancer in epidemiological and experimental studies. Various studies have shown that RAS blockage is protective in some cancers. However, although fewer, contradictory data also showed that RAS blockage is either not related or adversely related to cancer. Although the reasons for these findings are not exactly known, different types of receptors and effectors in RAS may account for these findings. In the current review, we summarize the different RAS receptors and cancer development with regard to epidemiology, and pathogenesis including cell signaling pathways, apoptosis, genetic and epigenetic factors.

Keywords: Angiotensin; Apoptosis; Cancer; Cell signaling; Genetic.

Publication types

  • Review

MeSH terms

  • Angiotensin Receptor Antagonists / pharmacology*
  • Angiotensin-Converting Enzyme Inhibitors / pharmacology*
  • Apoptosis / physiology
  • Carcinogens / toxicity
  • Cell Proliferation / physiology
  • Drug Contamination
  • Epigenesis, Genetic*
  • Heart Failure / drug therapy
  • Humans
  • Hypertension / drug therapy
  • MicroRNAs / physiology
  • Neoplasms / epidemiology*
  • Neoplasms / etiology
  • Peptidyl-Dipeptidase A / genetics
  • Renin-Angiotensin System / drug effects
  • Renin-Angiotensin System / physiology*
  • Signal Transduction*

Substances

  • Angiotensin Receptor Antagonists
  • Angiotensin-Converting Enzyme Inhibitors
  • Carcinogens
  • MicroRNAs
  • Peptidyl-Dipeptidase A