Revealing the Role of High-Density Lipoprotein in Colorectal Cancer

Int J Mol Sci. 2021 Mar 25;22(7):3352. doi: 10.3390/ijms22073352.

Abstract

Colorectal cancer (CRC) is a highly prevalent malignancy with multifactorial etiology, which includes metabolic alterations as contributors to disease development. Studies have shown that lipid status disorders are involved in colorectal carcinogenesis. In line with this, previous studies have also suggested that the serum high-density lipoprotein cholesterol (HDL-C) level decreases in patients with CRC, but more recently, the focus of investigations has shifted toward the exploration of qualitative properties of HDL in this malignancy. Herein, a comprehensive overview of available evidences regarding the putative role of HDL in CRC will be presented. We will analyze existing findings regarding alterations of HDL-C levels but also HDL particle structure and distribution in CRC. In addition, changes in HDL functionality in this malignancy will be discussed. Moreover, we will focus on the genetic regulation of HDL metabolism, as well as the involvement of HDL in disturbances of cholesterol trafficking in CRC. Finally, possible therapeutic implications related to HDL will be presented. Given the available evidence, future studies are needed to resolve all raised issues concerning the suggested protective role of HDL in CRC, its presumed function as a biomarker, and eventual therapeutic approaches based on HDL.

Keywords: HDL functional properties; HDL particle distribution; cholesterol trafficking; colorectal cancer; genetic background; high-density lipoprotein; therapeutic implications.

Publication types

  • Review

MeSH terms

  • Animals
  • Apolipoprotein A-I / metabolism
  • Apolipoproteins M / metabolism
  • Aryldialkylphosphatase / metabolism
  • Biomarkers / metabolism
  • Carcinogenesis
  • Cholesterol / metabolism
  • Cholesterol Ester Transfer Proteins / metabolism
  • Cholesterol, HDL / metabolism
  • Colorectal Neoplasms / metabolism*
  • Homeostasis
  • Humans
  • Lipoproteins, HDL / metabolism*
  • Mice
  • Polymorphism, Single Nucleotide
  • Precision Medicine
  • Scavenger Receptors, Class B / metabolism

Substances

  • APOA1 protein, human
  • Apolipoprotein A-I
  • Apolipoproteins M
  • Biomarkers
  • CETP protein, human
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Lipoproteins, HDL
  • SCARB1 protein, human
  • Scavenger Receptors, Class B
  • Cholesterol
  • Aryldialkylphosphatase
  • PON1 protein, human