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Artikel: ErbB-2 induces the cyclin D1 gene in prostate epithelial cells in vitro and in vivo.

Casimiro, Mathew / Rodriguez, Olga / Pootrakul, Llana / Aventian, Maral / Lushina, Nadia / Cromelin, Caroline / Ferzli, Georgina / Johnson, Kevin / Fricke, Stanley / Diba, Fantahun / Kallakury, Bhaskar / Ohanyerenwa, Chioma / Chen, Maxine / Ostrowski, Michael / Hung, Mien-Chie / Rabbani, Shafaat A / Datar, Ram / Cote, Richard / Pestell, Richard /
Albanese, Chris

Cancer research

2007  Band 67, Heft 9, Seite(n) 4364–4372

Abstract: The receptor tyrosine kinase ErbB-2 plays an important role in the regulation of growth factor-induced signal transduction cascades in the epithelium, and ErbB-2 is frequently overexpressed in epithelial tumors. Our previous studies on clinical prostate ... ...

Abstract The receptor tyrosine kinase ErbB-2 plays an important role in the regulation of growth factor-induced signal transduction cascades in the epithelium, and ErbB-2 is frequently overexpressed in epithelial tumors. Our previous studies on clinical prostate cancer specimens indicated that ErbB-2 expression was increased in patients undergoing hormone ablation therapy. We had also shown that the critical cell cycle regulatory gene cyclin D1 and its promoter were targets of proliferative signaling in prostate cancer cell lines, and that cyclin D1 was required for ErbB-2-induced mammary tumorigenesis. In the current studies, we found that increased ErbB-2 membrane expression correlated with increased nuclear cyclin D1 staining in clinical prostate cancer specimens, and that expression of ErbB-2 was capable of inducing cell cycle progression in human prostate cancer cell lines. We further showed that ErbB-2 induced the cyclin D1 promoter in DU145 cells, and that small interfering RNA knockdown of cyclin D1 protein levels blocked a significant proportion of the heregulin-induced cell cycle progression in LNCaP cells. Probasin promoter-targeted expression of an activated ErbB-2 isoform induced cyclin D1 expression in the mouse prostate, commensurate with prostate intraepithelial neoplasia. Together, these in vitro and in vivo studies identify cyclin D1 as a critical downstream target of ErbB-2 in the prostate epithelium, both of which are possible therapeutic targets for cancer intervention. Furthermore, our novel mouse model provides a useful platform for ongoing in vivo investigations of ErbB-2 signaling in the prostate epithelium.
Mesh-Begriff(e) Animals ; Cell Cycle/physiology ; Cell Growth Processes/physiology ; Cell Line, Tumor ; Cyclin D1/biosynthesis ; Cyclin D1/genetics ; Epithelial Cells/pathology ; Gene Expression Regulation, Neoplastic ; Genes, bcl-1 ; Humans ; Male ; Mice ; Promoter Regions, Genetic ; Prostatic Intraepithelial Neoplasia/genetics ; Prostatic Intraepithelial Neoplasia/metabolism ; Prostatic Intraepithelial Neoplasia/pathology ; Prostatic Neoplasms/genetics ; Prostatic Neoplasms/metabolism ; Prostatic Neoplasms/pathology ; RNA, Small Interfering/genetics ; Receptor, ErbB-2/biosynthesis
Chemische Substanzen RNA, Small Interfering ; Cyclin D1 (136601-57-5) ; Receptor, ErbB-2 (EC 2.7.10.1)
Sprache Englisch
Erscheinungsdatum 2007-05-01
Erscheinungsland United States
Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID 1432-1
ISSN 1538-7445 ; 0008-5472
ISSN (online) 1538-7445
ISSN 0008-5472
DOI 10.1158/0008-5472.CAN-06-1898
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