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Oleic acid induces ERK1/2 activation and AP-1 DNA binding activity through a mechanism involving Src kinase and EGFR transactivation in breast cancer cells.
- Source :
-
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2008 Nov 06; Vol. 294 (1-2), pp. 81-91. Date of Electronic Publication: 2008 Aug 15. - Publication Year :
- 2008
-
Abstract
- GPR40 and GPR120 are G-protein-coupled receptors that can be activated by medium- and long-chain fatty acids. GPR40 is expressed in several breast cancer cell lines and its stimulation with oleic acid (OA) induces cell proliferation. However, the signal transduction pathways activated by OA have not been studied in detail. Our results demonstrate that both GPR40 and GPR120 are expressed in MCF-7 cells. Stimulation of MCF-7 and MDA-MB-231 cells with OA promoted the phosphorylation of ERK1/2 at Thr-202 and Tyr-204 and the formation of AP-1-DNA complex in a fashion dependent of Src kinase activity and EGFR transactivation. Furthermore, proliferation induced by OA is restricted to breast cancer cells in a fashion dependent of ERK1/2 activation and matrix metalloproteinases. In summary, our data indicate that proliferation induced by OA is restricted to breast cancer cells, and that ERK1/2 activation and AP-1-DNA complex formation are mediated by Src family kinases and transactivation of EGFR.
- Subjects :
- Breast Neoplasms pathology
Cell Line, Tumor
Cell Proliferation drug effects
DNA, Neoplasm metabolism
Enzyme Activation drug effects
Humans
Matrix Metalloproteinases metabolism
Mitogen-Activated Protein Kinase 1 metabolism
Mitogen-Activated Protein Kinase 3 metabolism
Protein Binding drug effects
Receptors, G-Protein-Coupled metabolism
Breast Neoplasms enzymology
ErbB Receptors genetics
Extracellular Signal-Regulated MAP Kinases metabolism
Oleic Acid pharmacology
Transcription Factor AP-1 metabolism
Transcriptional Activation drug effects
src-Family Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0303-7207
- Volume :
- 294
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Molecular and cellular endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 18775472
- Full Text :
- https://doi.org/10.1016/j.mce.2008.08.003