Overlapping molecular pathways between cannabinoid receptors type 1 and 2 and estrogens/androgens on the periphery and their involvement in the pathogenesis of common diseases (Review)

Int J Mol Med. 2016 Dec;38(6):1642-1651. doi: 10.3892/ijmm.2016.2779. Epub 2016 Oct 17.

Abstract

The physiological and pathophysiological roles of sex hormones have been well documented and the modulation of their effects is applicable in many current treatments. On the other hand, the physiological role of endocannabinoids is not yet clearly understood and the endocannabinoid system is considered a relatively new therapeutic target. The physiological association between sex hormones and cannabinoids has been investigated in several studies; however, its involvement in the pathophysiology of common human diseases has been studied separately. Herein, we present the first systematic review of molecular pathways that are influenced by both the cannabinoids and sex hormones, including adenylate cyclase and protein kinase A, epidermal growth factor receptor, cyclic adenosine monophosphate response element-binding protein, vascular endothelial growth factor, proto-oncogene serine/threonine-protein kinase, mitogen-activated protein kinase, phosphatidylinositol-4,5-bisphosphate 3-kinase, C-Jun N-terminal kinase and extracellular-signal-regulated kinases 1/2. Most of these influence cell proliferative activity. Better insight into this association may prove to be beneficial for the development of novel pharmacological treatment strategies for many common diseases, including breast cancer, endometrial cancer, prostate cancer, osteoporosis and atherosclerosis. The associations between cannabinoids, estrogens and androgens under these conditions are also presented and the molecular interactions are highlighted.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Androgens / metabolism*
  • Animals
  • Cannabinoids / metabolism
  • Disease Susceptibility*
  • Estrogens / metabolism*
  • Humans
  • Proto-Oncogene Mas
  • Receptor, Cannabinoid, CB1 / metabolism*
  • Receptor, Cannabinoid, CB2 / metabolism*
  • Signal Transduction*

Substances

  • Androgens
  • Cannabinoids
  • Estrogens
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Receptor, Cannabinoid, CB1
  • Receptor, Cannabinoid, CB2