Lipoxin A4 and its analog suppress hepatocellular carcinoma via remodeling tumor microenvironment

Cancer Lett. 2011 Oct 1;309(1):85-94. doi: 10.1016/j.canlet.2011.05.020. Epub 2011 Jun 16.

Abstract

Macrophages play an important role in tumor inflammatory microenvironment, lipoxin (LX), the 'stop signal' for inflammation, has been extensively studied preclinically for its anti-inflammatory or inflammatory pro-resolving effect. Here, we showed that LXA(4) could promote the apoptosis and inhibit the proliferation, migration and angiogenesis of HepG2 hepatocarcinoma cells stimulated by lipopolysaccharide (LPS) or activated macrophage-conditioned media (ACM). Moreover, BML-111, the analog of LXA(4), effectively inhibited the proliferation, invasion and angiogenesis of tumor in H22 hepatocarcinoma cell bearing mice. These results showed that LXA(4) could be a possible candidate for liver cancer therapy, and blocking the activation of macrophages would be an effective drug target.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Carcinoma, Hepatocellular* / blood supply
  • Carcinoma, Hepatocellular* / drug therapy
  • Carcinoma, Hepatocellular* / pathology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Culture Media, Conditioned
  • Heptanoic Acids / pharmacology
  • Humans
  • Lipoxins / chemistry
  • Lipoxins / metabolism*
  • Lipoxins / pharmacology
  • Liver Neoplasms* / blood supply
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / pathology
  • Macrophages / metabolism
  • Macrophages / pathology
  • Male
  • Mice
  • Neoplasm Transplantation
  • Neovascularization, Pathologic / drug therapy
  • Tumor Microenvironment / drug effects

Substances

  • 5(S),6(R)-7-trihydroxyheptanoic acid, methyl ester
  • Culture Media, Conditioned
  • Heptanoic Acids
  • Lipoxins
  • lipoxin A4