Brief Communication
Green tea catechin extract in intervention of chronic breast cell carcinogenesis induced by environmental carcinogens
Article first published online: 31 AUG 2011
DOI: 10.1002/mc.20844
Copyright © 2011 Wiley Periodicals, Inc.
Issue

Molecular Carcinogenesis
Special Issue: Theme Issue: Phytochemicals for the Prevention and Treatment of Cancer
Volume 51, Issue 3, pages 280–289, March 2012
Additional Information
How to Cite
Rathore, K. and Wang, H.-C. R. (2012), Green tea catechin extract in intervention of chronic breast cell carcinogenesis induced by environmental carcinogens. Mol. Carcinog., 51: 280–289. doi: 10.1002/mc.20844
Publication History
- Issue published online: 12 JAN 2012
- Article first published online: 31 AUG 2011
- Manuscript Accepted: 22 JUL 2011
- Manuscript Revised: 11 JUL 2011
- Manuscript Received: 6 MAY 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- breast cancer;
- dietary prevention;
- reactive oxygen species;
- ERK;
- DNA damage
Abstract
Sporadic breast cancers are mainly attributable to long-term exposure to environmental factors, via a multi-year, multi-step, and multi-path process of tumorigenesis involving cumulative genetic and epigenetic alterations in the chronic carcinogenesis of breast cells from a non-cancerous stage to precancerous and cancerous stages. Epidemiologic and experimental studies have suggested that green tea components may be used as preventive agents for breast cancer control. In our research, we have developed a cellular model that mimics breast cell carcinogenesis chronically induced by cumulative exposures to low doses of environmental carcinogens. In this study, we used our chronic carcinogenesis model as a target system to investigate the activity of green tea catechin extract (GTC) at non-cytotoxic levels in intervention of cellular carcinogenesis induced by cumulative exposures to pico-molar 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and benzo[a]pyrene (B[a]P). We identified that GTC, at a non-cytotoxic, physiologically achievable concentration of 2.5 µg/mL, was effective in suppressing NNK- and B[a]P-induced cellular carcinogenesis, as measured by reduction of the acquired cancer-associated properties of reduced dependence on growth factors, anchorage-independent growth, increased cell mobility, and acinar-conformational disruption. We also detected that intervention of carcinogen-induced elevation of reactive oxygen species (ROS), increase of cell proliferation, activation of the ERK pathway, DNA damage, and changes in gene expression may account for the mechanisms of GTC's preventive activity. Thus, GTC may be used in dietary and chemoprevention of breast cell carcinogenesis associated with long-term exposure to low doses of environmental carcinogens. © 2011 Wiley Periodicals, Inc.

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