Alteration at transcriptional level of cardiac renin-angiotensin system by letrozole treatment

Acta Cardiol. 2019 Apr;74(2):109-113. doi: 10.1080/00015385.2018.1472840. Epub 2018 Jun 17.

Abstract

Introduction: The use of aromatase inhibitors (AIs) for breast cancer led to a marked change in ventricular function. Since accumulating evidence indicates that overactivation of the cardiac renin-angiotensin system (RAS) plays an important role in the development of cardiovascular diseases such as hypertrophy and remodelling, we aimed to investigate whether letrozole alters the transcription level of RAS related genes in the cardiac tissue.

Methods: Twenty four rats were randomly divided into four groups (n = 6 per group): two groups were letrozole treated (1 and 2 mg/kg/day orally), one group was vehicle treated (DMSO) and one group was the control group without any treatment. 12 weeks after beginning treatment with letrozole, we examined the rate of transcription of renin, angiotensinogen, AngII type 1a and 1b (AT1a and AT1b) and type 2 receptors (AT2) in the rat heart using real-time polymerase chain reaction.

Results: The cardiac mRNA levels of several components of the RAS in the rats treated with letrozole were significantly increased including AT1a receptor (80%), renin (51%), and angiotensinogen (33%). Though not significant, AT2 receptor levels were observed to decrease with increasing doses of letrozole.

Conclusions: Letrozole can induce significant changes in some RAS related genes. These alterations are important to understand the pathways and consequences beyond cardiac events induced by breast cancer treatments.

Keywords: Renin-Angiotensin system; breast cancer; cardiac disease; gene Transcription; letrozole.

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Disease Models, Animal
  • Female
  • Heart Diseases* / drug therapy
  • Heart Diseases* / genetics
  • Heart Diseases* / metabolism
  • Letrozole* / therapeutic use
  • Myocardium* / metabolism
  • RNA, Messenger* / genetics
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Real-Time Polymerase Chain Reaction
  • Renin-Angiotensin System* / genetics
  • Transcription, Genetic / drug effects

Substances

  • Antineoplastic Agents
  • Letrozole
  • RNA, Messenger