Targeting cellular cholesterol for anticancer therapy

FEBS J. 2019 Nov;286(21):4192-4208. doi: 10.1111/febs.15018. Epub 2019 Aug 12.

Abstract

Cholesterol dyshomeostasis in cancer cells leads to intracellular cholesterol accumulation, which imparts drug resistance and allows these cells to evade apoptotic signalling processes and maintain continuous cell division and proliferation. Therefore, cholesterol lowering in cancer cells has been envisaged as a potential anticancer strategy. In this direction, two therapeutic strategies have been proposed: (a) to inhibit the biosynthesis of cholesterol in the cells and (b) to deplete excess cholesterol from cancer cells. In the first phase of this review, we collate the cancer signalling pathways (particularly in breast cancer) that are perturbed by cholesterol dyshomeostasis and highlight recent drug discovery efforts to develop cholesterol-lowering compounds, some of which are currently under clinical trials. In the second phase, based on the analysis of the available scientific evidence, we conceptualize and argue that the depletion of excess cholesterol could sensitize cancer cells to available therapeutics and may also help to alleviate cancer drug resistance.

Keywords: breast cancer; cholesterol depletion; cholesterol regulation; metabolic and signalling pathways; statins.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Apoptosis / drug effects
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cholesterol / genetics
  • Cholesterol / metabolism*
  • Drug Resistance, Neoplasm / drug effects
  • Female
  • Homeostasis / genetics*
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Signal Transduction / genetics

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Cholesterol