Heparanase: A Novel Therapeutic Target for the Treatment of Atherosclerosis

Cells. 2022 Oct 12;11(20):3198. doi: 10.3390/cells11203198.

Abstract

Cardiovascular disease (CVD) is the leading cause of death and disability worldwide, and its management places a huge burden on healthcare systems through hospitalisation and treatment. Atherosclerosis is a chronic inflammatory disease of the arterial wall resulting in the formation of lipid-rich, fibrotic plaques under the subendothelium and is a key contributor to the development of CVD. As such, a detailed understanding of the mechanisms involved in the development of atherosclerosis is urgently required for more effective disease treatment and prevention strategies. Heparanase is the only mammalian enzyme known to cleave heparan sulfate of heparan sulfate proteoglycans, which is a key component of the extracellular matrix and basement membrane. By cleaving heparan sulfate, heparanase contributes to the regulation of numerous physiological and pathological processes such as wound healing, inflammation, tumour angiogenesis, and cell migration. Recent evidence suggests a multifactorial role for heparanase in atherosclerosis by promoting underlying inflammatory processes giving rise to plaque formation, as well as regulating lesion stability. This review provides an up-to-date overview of the role of heparanase in physiological and pathological processes with a focus on the emerging role of the enzyme in atherosclerosis.

Keywords: atherosclerosis; extracellular matrix (ECM); heparan sulfate; heparanase; immune cells; inflammation.

Publication types

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

MeSH terms

  • Animals
  • Atherosclerosis* / therapy
  • Glucuronidase
  • Heparan Sulfate Proteoglycans
  • Heparitin Sulfate
  • Humans
  • Lipids
  • Mammals
  • Plaque, Atherosclerotic* / therapy

Substances

  • heparanase
  • Heparan Sulfate Proteoglycans
  • Glucuronidase
  • Heparitin Sulfate
  • Lipids

Grants and funding

This work was supported by the Medical Research Future Fund Cardiovascular Health Mission Grant (MRF2008787).