3-O-Methylfunicone, a metabolite produced by Penicillium pinophilum, modulates ERK1/2 activity, affecting cell motility of human mesothelioma cells.

Abstract

OBJECTIVES:

3-O-methylfunicone (OMF), a secondary metabolite produced by Penicillium pinophilum, affects cell proliferation and motility in a variety of human solid tumours. The aim of this study was to demonstrate whether OMF has the ability to arrest cell division and motility, in a human mesothelioma cell line. Malignant mesothelioma is an aggressive cancer that does not respond to standard therapies the cells of which are considered to be highly resistant to apoptosis.

MATERIAL AND METHODS:

Cell motility and invasion were measured using a modified Boyden chamber. Gene expression was examined by RT-PCR, while ERK1/2 was investigated by Western blot analysis. All experiments were also performed on primary cultures of mesothelial cells.

RESULTS:

The present study shows that OMF inhibited motility of the NCI mesothelioma cell line by modulating ERK signalling activity, and affected alphaVbeta5 integrin and MMP-2 expression, inducing marked downregulation at both mRNA and protein levels. Substantial downregulation of VEGF gene expression was also demonstrated. These effects were not observed in normal mesothelial cell cultures.

CONCLUSION:

OMF may have potential as a naturally derived anti-tumour drug for treatment of mesothelioma.

• Authors: E Buommino, I Paoletti, A De Filippis, R Nicoletti, M L Ciavatta, S Menegozzo, M Menegozzo, M A Tufano
• Journal: Cell proliferation (Cell Prolif) Vol. 43 Issue 2 Pg. 114-23 (Apr 2010) ISSN: 1365-2184 [Electronic] England
• PMID: 20447056 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• 3-O-methylfunicone
• Pyrones
• Receptors, Vitronectin
• integrin alphaVbeta5
• Mitogen-Activated Protein Kinase 1
• Mitogen-Activated Protein Kinase 3
• Matrix Metalloproteinase 2

Topics

• Cell Line, Tumor
• Cell Movement (drug effects)
• Down-Regulation
• Humans
• Matrix Metalloproteinase 2 (metabolism)
• Mesothelioma (genetics, metabolism)
• Mitogen-Activated Protein Kinase 1 (metabolism)
• Mitogen-Activated Protein Kinase 3 (metabolism)
• Penicillium (metabolism)
• Pyrones (pharmacology)
• Receptors, Vitronectin (metabolism)
• Signal Transduction (genetics)