Hyperinsulinaemia in cancer

Nat Rev Cancer. 2020 Nov;20(11):629-644. doi: 10.1038/s41568-020-0295-5. Epub 2020 Sep 9.

Abstract

Elevated circulating insulin levels are frequently observed in the setting of obesity and early type 2 diabetes, as a result of insensitivity of metabolic tissues to the effects of insulin. Higher levels of circulating insulin have been associated with increased cancer risk and progression in epidemiology studies. Elevated circulating insulin is believed to be a major factor linking obesity, diabetes and cancer. With the development of targeted cancer therapies, insulin signalling has emerged as a mechanism of therapeutic resistance. Although metabolic tissues become insensitive to insulin in the setting of obesity, a number of mechanisms allow cancer cells to maintain their ability to respond to insulin. Significant progress has been made in the past decade in understanding the insulin receptor and its signalling pathways in cancer, and a number of lessons have been learnt from therapeutic failures. These discoveries have led to numerous clinical trials that have aimed to reduce the levels of circulating insulin and to abrogate insulin signalling in cancer cells. With the rising prevalence of obesity and diabetes worldwide, and the realization that hyperinsulinaemia may contribute to therapeutic failures, it is essential to understand how insulin and insulin receptor signalling promote cancer progression.

Publication types

  • Review

MeSH terms

  • Antigens, CD / metabolism*
  • Comorbidity
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / epidemiology
  • Diabetes Mellitus, Type 2 / metabolism*
  • Drug Resistance, Neoplasm / physiology
  • Humans
  • Hyperinsulinism / blood
  • Hyperinsulinism / epidemiology
  • Hyperinsulinism / metabolism*
  • Insulin / blood
  • Insulin / metabolism
  • Insulin Resistance* / physiology
  • Neoplasms / blood
  • Neoplasms / epidemiology
  • Neoplasms / metabolism*
  • Obesity / blood
  • Obesity / epidemiology
  • Obesity / metabolism*
  • Receptor, Insulin / metabolism*
  • Signal Transduction

Substances

  • Antigens, CD
  • Insulin
  • INSR protein, human
  • Receptor, Insulin