In this study, we have evaluated the effects of extracellular magnesium restriction on the growth and cell cycle parameters of normal (HC11) and transformed (MCF-7) breast epithelial cell lines. Cells were incubated in medium with different concentrations of Mg2+ (from 0.5 to 0 mM) and the growth ra
Increased expression of MDM2, cyclin D1, and p27Kip1 in carcinogen-induced rat mammary tumors
✍ Scribed by Stephen A. Murray; Shi Yang; Elizabeth Demicco; Haoqiang Ying; David H. Sherr; Laurie J. Hafer; Adrianne E. Rogers; Gail E. Sonenshein; Zhi-Xiong Jim Xiao
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 274 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0730-2312
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✦ Synopsis
Abstract
It is thought that environmental pollutants, such as polycyclic aromatic hydrocarbons (PAH), contribute to human breast tumorigenesis, yet their roles remain incompletely elucidated. The prototypical PAH 7,12‐dimethylbenz(α)anthracene (DMBA) specifically and effectively induces mammary tumor formation in rodent models. In an attempt to explore the molecular mechanisms by which PAH initiates and promotes mammary tumorigenesis, we examined the expression of several cell cycle regulators in rat mammary tumors induced by DMBA. Expression of cyclin D1, murine double minute‐2 (MDM2), and Akt was up‐regulated in tumors in comparison to normal mammary glands, as indicated by RT‐PCR, Western blot analysis, and immunohistochemical staining. Expression of p27^Kip1^ protein was also elevated in the tumors with increased cytoplasmic localization. However, RB protein remained hyperphosphorylated. To directly test the effects of DMBA, the MCF‐7 human breast cancer cells were treated. DMBA induced MDM2 expression in a dose‐ and time‐dependent fashion in the MCF‐7 cells, and this activation appeared to be p53 dependent. These data suggest that activation of cyclin D1, MDM2, and AKT as well as increased expression and cytoplasmic localization of p27^Kip1^ may play a role in this model of environmental pollutant‐induced mammary tumorigenesis. © 2005 Wiley‐Liss, Inc.
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