Published September 30, 2008 | Version v1
Journal article

The fatty acid binding protein 7 (FABP7) is involved in proliferation and invasion of melanoma cells

  • 1. Pathology Clinic, Rikshospitalet-Radiumhospitalet Medical Center, Montebello N-0310 Oslo (Norway)
  • 2. Faculty Division Radiumhospitalet, Medical Faculty, University of Oslo, Oslo (Norway)

Description

The molecular mechanisms underlying melanoma tumor development and progression are still not completely understood. One of the new candidates that emerged from a recent gene expression profiling study is fatty acid-binding protein 7 (FABP7), involved in lipid metabolism, gene regulation, cell growth and differentiation. We studied the functional role of FABP7 in human melanoma cell lines and using immunohistochemistry analyzed its expression pattern and clinical role in 11 nevi, 149 primary melanomas and 68 metastases. FABP7 mRNA and protein level is down-regulated following treatment of melanoma cell lines with a PKC activator (PMA) or MEK1 inhibitor (PD98059). Down-regulation of FABP7 using siRNA decreased cell proliferation and invasion but did not affect apoptosis. In clinical specimens, FABP7 was expressed in 91% of nevi, 71% of primary melanomas and 70% of metastases, with a cytoplasmic and/or nuclear localization. FABP7 expression was associated with tumor thickness in superficial spreading melanoma (P = 0.021). In addition, we observed a trend for an association between FABP7 expression and Ki-67 score (P = 0.070) and shorter relapse-free survival (P = 0.069) in this group of patients. Our data suggest that FABP7 can be regulated by PKC and the MAPK/ERK1/2 pathway through independent mechanisms in melanoma cell lines. Furthermore, FABP7 is involved in cell proliferation and invasion in vitro, and may be associated with tumor progression in melanoma

Availability note (English)

Available from http://dx.doi.org/10.1186/1471-2407-8-276; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2569959

Additional details

Publishing Information

Journal Title
BMC Cancer (Online)
Journal Volume
8
Journal Page Range
p. 276
ISSN
1471-2407

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46092051
Subject category
S60: APPLIED LIFE SCIENCES; S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
APOPTOSIS; CARBOXYLIC ACIDS; CELL PROLIFERATION; GENE REGULATION; GENES; IN VITRO; LIPIDS; MELANOMAS; METABOLISM; METASTASES; PATIENTS; PROTEINS; REGULATIONS; THICKNESS
Descriptors DEC
CARCINOMAS; DIMENSIONS; DISEASES; EPITHELIOMAS; LAWS; NEOPLASMS; ORGANIC ACIDS; ORGANIC COMPOUNDS

Optional Information

Copyright
Copyright (c) 2008 Slipicevic et al
Notes
PMCID: PMC2569959; PUBLISHER-ID: 1471-2407-8-276; PMID: 18826602; OAI: oai:pubmedcentral.nih.gov:2569959; licensee BioMed Central Ltd.