Abstract |
1,25(OH)(2)D(3) antiproliferative properties are widely known. However, the molecular bases of these properties are only partially elucidated. Since 1,25(OH)(2)D(3) effectively arrests growth in many tumors and hyperplastic tissues whose growth is driven by co-expression of EGFR and its ligand TGF-alpha, it was hypothesized that 1,25(OH)(2)D(3) could affect the TGF-alpha/EGFR-autocrine growth loop. This study examined 1,25(OH)(2)D(3) regulation of EGFR-growth signals, using human epidermoid A431 cells, in which the overexpression of EGFR and TGF-alpha constitute the major autocrine mitogenic signal. 1,25(OH)(2)D(3) inhibited autocrine and EGF-induced A431 cell proliferation. Furthermore, 1,25(OH)(2)D(3) changed the cellular localization of both TGF-alpha and EGFR and inhibited ligand-dependent phosphorylation of EGFR and ERK1/2. In addition, 1,25(OH)(2)D(3) impaired autocrine and EGF-induced nuclear translocation of activated EGFR and, consequently, its binding to AT-rich DNA sequences and transcriptional activation of the cyclin D1 promoter. These results demonstrate that 1,25(OH)(2)D(3) alters EGFR membrane trafficking and down-regulates EGFR growth signaling.
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Authors | Julia B Cordero, Mario Cozzolino, Yan Lu, Marcos Vidal, Eduardo Slatopolsky, Philip D Stahl, M Alejandro Barbieri, Adriana Dusso |
Journal | The Journal of biological chemistry
(J Biol Chem)
Vol. 277
Issue 41
Pg. 38965-71
(Oct 11 2002)
ISSN: 0021-9258 [Print] United States |
PMID | 12181310
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Transforming Growth Factor alpha
- Cyclin D1
- ErbB Receptors
- Mitogen-Activated Protein Kinases
- Calcitriol
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Topics |
- Animals
- Calcitriol
(metabolism)
- Cell Division
(physiology)
- Cell Membrane
(metabolism)
- Cell Nucleus
(metabolism)
- Cyclin D1
(genetics)
- Down-Regulation
- Enzyme Activation
- ErbB Receptors
(metabolism)
- Humans
- Immunohistochemistry
- Mitogen-Activated Protein Kinases
(metabolism)
- Promoter Regions, Genetic
- Signal Transduction
(physiology)
- Time Factors
- Transforming Growth Factor alpha
(metabolism)
- Tumor Cells, Cultured
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