Diminished lipocalin-type prostaglandin D(2) synthase expression in human lung tumors

Lung Cancer. 2010 Oct;70(1):103-9. doi: 10.1016/j.lungcan.2010.01.011. Epub 2010 Feb 7.

Abstract

Previously, we demonstrated that lipocalin-type prostaglandin D(2) synthase (L-PGDS) induces apoptosis and prevents cell cycle progression in several cell types. In this study we determined the expression of L-PGDS in a variety of human lung tumor types. While L-PGDS expression was evident in the surrounding margins, we observed significantly decreased protein and gene expression in the tumor tissue. Using RT-PCR we demonstrated that L-PGDS gene expression decreased proportionately with tumor progression. In addition, we demonstrated that exogenously added L-PGDS could suppress the hyperproliferation and PDGF-stimulated migration of A549 cells, a cultured carcinomic human alveolar basal epithelial cell line. We conclude that L-PGDS may play a key role in modulating lung cancer growth and may offer a novel diagnostic and therapeutic approach for treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma, Bronchiolo-Alveolar / enzymology
  • Adenocarcinoma, Bronchiolo-Alveolar / genetics
  • Adenocarcinoma, Bronchiolo-Alveolar / pathology
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Carcinoma, Non-Small-Cell Lung / enzymology
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Cell Growth Processes / drug effects
  • Cell Growth Processes / physiology
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Movement / physiology
  • Disease Progression
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Intramolecular Oxidoreductases / biosynthesis*
  • Intramolecular Oxidoreductases / deficiency
  • Intramolecular Oxidoreductases / genetics
  • Intramolecular Oxidoreductases / pharmacology
  • Lipocalins / biosynthesis*
  • Lipocalins / genetics
  • Lipocalins / pharmacology
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Platelet-Derived Growth Factor / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Lipocalins
  • Platelet-Derived Growth Factor
  • Intramolecular Oxidoreductases
  • prostaglandin R2 D-isomerase