Controlling cancer through the autotaxin-lysophosphatidic acid receptor axis

Biochem Soc Trans. 2012 Feb;40(1):31-6. doi: 10.1042/BST20110608.

Abstract

LPA (lysophosphatidic acid, 1-acyl-2-hydroxy-sn-glycero-3-phosphate), is a growth factor-like lipid mediator that regulates many cellular functions, many of which are unique to malignantly transformed cells. The simple chemical structure of LPA and its profound effects in cancer cells has attracted the attention of the cancer therapeutics field and drives the development of therapeutics based on the LPA scaffold. In biological fluids, LPA is generated by ATX (autotaxin), a lysophospholipase D that cleaves the choline/serine headgroup from lysophosphatidylcholine and lysophosphatidylserine to generate LPA. In the present article, we review some of the key findings that make the ATX-LPA signalling axis an emerging target for cancer therapy.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Humans
  • Lysophospholipids / metabolism
  • Molecular Targeted Therapy
  • Neoplasm Invasiveness
  • Neoplasms / drug therapy
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Organophosphonates / pharmacology
  • Organophosphonates / therapeutic use
  • Phosphodiesterase Inhibitors / pharmacology
  • Phosphodiesterase Inhibitors / therapeutic use
  • Phosphoric Diester Hydrolases / genetics
  • Phosphoric Diester Hydrolases / metabolism*
  • Receptors, Lysophosphatidic Acid / metabolism*
  • Signal Transduction
  • Xenograft Model Antitumor Assays

Substances

  • 4-pentadecylbenzylphosphonic acid
  • Antineoplastic Agents
  • Lysophospholipids
  • Organophosphonates
  • Phosphodiesterase Inhibitors
  • Receptors, Lysophosphatidic Acid
  • Phosphoric Diester Hydrolases
  • alkylglycerophosphoethanolamine phosphodiesterase
  • lysophosphatidic acid