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.
Copyright 2010 Elsevier Ireland Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenocarcinoma, Bronchiolo-Alveolar / enzymology
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Adenocarcinoma, Bronchiolo-Alveolar / genetics
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Adenocarcinoma, Bronchiolo-Alveolar / pathology
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Apoptosis / drug effects
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Apoptosis / physiology
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Carcinoma, Non-Small-Cell Lung / enzymology
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Carcinoma, Non-Small-Cell Lung / genetics
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Carcinoma, Non-Small-Cell Lung / pathology
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Cell Growth Processes / drug effects
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Cell Growth Processes / physiology
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Cell Line, Tumor
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Cell Movement / drug effects
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Cell Movement / physiology
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Disease Progression
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Gene Expression Regulation, Enzymologic
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Gene Expression Regulation, Neoplastic
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Humans
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Intramolecular Oxidoreductases / biosynthesis*
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Intramolecular Oxidoreductases / deficiency
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Intramolecular Oxidoreductases / genetics
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Intramolecular Oxidoreductases / pharmacology
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Lipocalins / biosynthesis*
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Lipocalins / genetics
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Lipocalins / pharmacology
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Lung Neoplasms / enzymology*
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Lung Neoplasms / genetics
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Lung Neoplasms / pathology
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Platelet-Derived Growth Factor / pharmacology
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Reverse Transcriptase Polymerase Chain Reaction
Substances
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Lipocalins
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Platelet-Derived Growth Factor
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Intramolecular Oxidoreductases
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prostaglandin R2 D-isomerase