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Published on: July 5, 2017
Molecular targets for the cancer preventive activity of tea polyphenols
Chung S Yang1, Joshua D Lambert, Zhe Hou
1Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA.
Abstract:
Inhibition of carcinogenesis by tea and tea polyphenols has been demonstrated in many animal models. The mechanisms of action have been extensively investigated mostly in cell culture systems with (-)-epigallocatechin-3-gallate (EGCG), the most active and major polyphenolic compound from green tea. However, the mechanisms of cancer preventive activity by tea and tea polyphenols are not clearly understood. This article discusses some of the reported mechanisms and possible targets for the action of EGCG. The difficulties and major issues in extrapolating data from studies in cancer cell lines to cancer prevention mechanisms are discussed. Activities observed in cell culture with high concentrations of EGCG may not be relevant because of the limited systemic bioavailability of EGCG. In addition, possible artifacts due to the auto-oxidation of EGCG may complicate this issue. Some recent studies revealed high-affinity EGCG binding proteins as possible direct targets for the action of EGCG. Validating the related cancer preventive mechanisms found in in vitro studies in animal models and human samples would be exciting.
Insights
Green tea
Area of Science:
- Nutritional Biochemistry
- Cancer Prevention Research
- Pharmacology
Background:
- Tea polyphenols, particularly epigallocatechin-3-gallate (EGCG) from green tea, show promise in inhibiting cancer.
- Existing research primarily uses cell culture models, leaving mechanisms of cancer prevention unclear.
Purpose of the Study:
- To discuss reported mechanisms and potential targets of EGCG in cancer prevention.
- To address challenges in translating in vitro findings to in vivo cancer prevention.
Main Methods:
- Review of existing literature on tea polyphenols and EGCG.
- Analysis of cell culture studies and their limitations.
- Discussion of bioavailability and potential artifacts like EGCG auto-oxidation.
Main Results:
- In vitro studies with high EGCG concentrations may not reflect in vivo efficacy due to limited bioavailability.
- EGCG auto-oxidation can complicate interpretation of cell culture results.
- Identification of high-affinity EGCG binding proteins suggests direct molecular targets.
Conclusions:
- Translating in vitro findings on EGCG's cancer preventive mechanisms to animal models and human studies is crucial.
- Further validation is needed to confirm the relevance of identified EGCG targets and mechanisms in real-world cancer prevention.
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