Leptin signalling, obesity and prostate cancer: molecular and clinical perspective on the old dilemma

Oncotarget. 2015 Nov 3;6(34):35556-63. doi: 10.18632/oncotarget.5574.

Abstract

The prevalence of global obesity is increasing. Obesity is associated with general cancer-related morbidity and mortality and is a known risk factor for development of specific cancers. A recent large systematic review of 24 studies based on meta-analysis of 11,149 patients with prostate cancer showed a significant correlation between obesity and the risk of advanced prostate cancer. Further, a sustained reduction in BMI correlates with a decreased risk of developing aggressive disease. On the other hand, the correlation between consuming different products and prostate cancer occurrence/risk is limited.Here, we review the role of adipose tissue from an endocrine perspective and outline the effect of adipokines on cancer metabolism, with particular focus on leptin. Leptin exerts its physiological and pathological effects through modification of intracellular signalling, most notably activating the Janus kinase (JAK) 2/signal transducer and activator of transcription (STAT) 3 pathway and recently shown sphingolipid pathway. Both high levels of leptin in circulation and leptin receptor mutation are associated with prostate cancer risk in human patients; however, the in vivo mechanistic evidence is less conclusive.Given the complexity of metabolic cancer pathways, it is possible that leptin may have varying effects on prostate cancer at different stages of its development, a point that may be addressed by further epidemiological studies.

Keywords: leptin; mortality; obesity; progression; prostate cancer.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Adipose Tissue / metabolism*
  • Adipose Tissue / pathology
  • Animals
  • Carcinogenesis
  • Genetic Predisposition to Disease
  • Humans
  • Janus Kinases / metabolism
  • Leptin / metabolism*
  • Male
  • Obesity / complications
  • Obesity / genetics
  • Obesity / metabolism*
  • Polymorphism, Genetic
  • Prostatic Neoplasms / complications
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism*
  • Receptors, Leptin / genetics
  • Receptors, Leptin / metabolism*
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction

Substances

  • Leptin
  • Receptors, Leptin
  • STAT3 Transcription Factor
  • Janus Kinases