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A cyclic peptide derived from ?-fetoprotein inhibits the proliferative effects of the epidermal growth factor and estradiol in MCF7 cells
Keywords: growth, inhibition, hormone, estrogens, expression, antibody, binding, culture, serum, protein, proliferation, cell, gene, matrix, alpha, release, cancer, metabolism, tumor, estradiol, humans, estrogen, human, receptor, strain, metalloproteinases, regulation, heparin, tissue, gelatinase, neoplasms, female, kinases, pathology, fetal, article, kinase, factor, breast, antineoplastic, activity, calf, controlled, fluorescent, metalloproteinase, technique, study, 7, western, priority, cyclic, journal, blotting, Blotting,, 2, a, cyclopeptide, Peptides,, Cells,, Cultured, Receptor,, erbB-2, medium, activated, b, epidermal, mitogen, Mitogen-Activated, alpha-Fetoproteins, fetoprotein, mcf
Abstract
A cyclic peptide derived from the active domain of ?-fetoprotein (AFP) significantly inhibited the proliferation of MCF7 cells stimulated with the epidermal growth factor (EGF) or estradiol (E 2). The action of these three agents on cell growth was independent of the presence of calf serum in the culture medium. Our results demonstrated that the cyclic peptide interfered markedly with the regulation of MAPK by activated c-erbB2. The cyclic peptide showed no effect on the E 2-stimulated release of matrix metalloproteinases 2 and 9 nor on the shedding of heparin-binding EGF into the culture medium. We propose that the AFP-derived cyclic peptide represents a valuable novel antiproliferative, agent for treating breast cancer.
Más información
| Título de la Revista: | ONCOLOGY REPORTS |
| Volumen: | 19 |
| Número: | 6 |
| Editorial: | SPANDIDOS PUBL LTD |
| Fecha de publicación: | 2008 |
| Página de inicio: | 1597 |
| Página final: | 1603 |
| URL: | http://www.scopus.com/inward/record.url?eid=2-s2.0-48849093305&partnerID=q2rCbXpz |