4.6 Review

Autotaxin, a secreted lysophospholipase D, as a promising therapeutic target in chronic inflammation and cancer

Journal

PROGRESS IN LIPID RESEARCH
Volume 58, Issue -, Pages 76-96

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.plipres.2015.02.001

Keywords

Autotaxin; Cancer; Inflammation; Inhibitors; Lysophosphatidic acid; Lysophospholipase D

Funding

  1. National SYNERGASIA Grant [09SYN-11-679]
  2. European Regional Development Fund
  3. National resources through the Operational Program Competitiveness and Entrepreneurship of the National Strategic Reference Framework (NSRF)

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Autotaxin (ATX) is a member of the nucleotide pyrophosphataSe/phosphodiesterase family of ectoenzymes that hydrolyzes phosphodiester bonds of various nucleotides. It possesses lysophospholipase D activity, catalyzing the hydrolysis of lysophosphatidylcholine into lysophosphatidic acid (LPA), and it is considered the major LPA-producing enzyme in the circulation. LPA is a bioactive phospholipid with diverse functions in almost every mammalian cell type, which exerts its action through binding to specific G protein-coupled receptors and stimulates various cellular functions, including migration, proliferation and survival. As a consequence, both ATX and LPA have attracted the interest of researchers, in an effort to understand their roles in physiology and pathophysiology. The present review article aims to summarize the existing knowledge as to the implications of ATX in chronic inflammatory diseases and cancer and to highlight the low molecular weight compounds, which have been developed as leads for the discovery of novel medicines to treat inflammatory diseases and cancer. (C) 2015 Elsevier Ltd. All rights reserved.

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