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[Molecular targets of tea polyphenols and its roles of anticancer drugs in experimental therapy]
1Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China. bjcsz@imb.pumc.edu.cn
Abstract:
Tea polyphenols (TPs), major biological active constituents of green tea, exert moderate and selective anticancer effects. Molecular mechanisms of TPs in cancer prevention and treatment involve multiple potential molecular targets. TPs inhibit growth factor receptor-mediated signal transduction pathway, decrease the activities of mitogen activated protein kinases and activator protein transcription factor-1, block nuclear factor-kappaB signaling pathway, reduce proteasome activity, lower overexpression of COX-2, subside dihydrofolate reductase and telomerase, and inhibit DNA methylation and matrix metalloproteinases. Furthermore, TPs enhance the inhibitory effect on the growth of cancers by traditional anticancer drugs or targeted antitumor drugs in vitro and in vivo and reverse multidrug resistances of cancer cells to vincristine, doxorubicin, and 5-fluorouracil. Besides, TPs reduce the nephrotoxicity induced by cisplatin, ameliorate irinotecan-induced side effects in the small intestine of mice, and decrease bleomycin-caused DNA damage in human leukocytes. TPs also increase antitumor activity of vaccine through immunological modulation. TPs play roles of the augmentation of antitumor effects, the reversal of multidrug resistance, and the reduction of side effects of chemotherapeutic drugs. TPs could be used as biochemical modulators in cancer therapy.
Insights
Green tea polyphenols (TPs) show anticancer effects by targeting multiple molecular pathways. TPs enhance chemotherapy efficacy, reverse drug resistance, and reduce treatment side effects.
Area of Science:
- Phytochemistry and Pharmacology
- Molecular Oncology
- Cancer Therapeutics
Context:
- Green tea polyphenols (TPs) are bioactive compounds with demonstrated anticancer properties.
- Understanding the molecular mechanisms of TPs is crucial for optimizing cancer prevention and treatment strategies.
- TPs interact with various cellular pathways implicated in cancer development and progression.
Purpose:
- To elucidate the multifaceted molecular mechanisms by which tea polyphenols (TPs) exert anticancer effects.
- To investigate the potential of TPs as adjuncts in cancer therapy, including their role in enhancing conventional treatments and overcoming drug resistance.
- To explore the protective effects of TPs against chemotherapy-induced toxicity.
Summary:
- Tea polyphenols (TPs) modulate key signaling pathways, including growth factor receptor pathways, MAPK, AP-1, NF-κB, and COX-2.
- TPs inhibit enzymes like dihydrofolate reductase and telomerase, and affect DNA methylation and matrix metalloproteinases.
- TPs enhance the efficacy of traditional and targeted anticancer drugs, reverse multidrug resistance, and mitigate chemotherapy-induced side effects like nephrotoxicity and DNA damage.
Impact:
- TPs demonstrate significant potential as biochemical modulators to augment antitumor effects and improve cancer treatment outcomes.
- The findings support the use of TPs to enhance the effectiveness of existing cancer therapies and reduce associated toxicities.
- TPs offer a promising natural compound-based approach for cancer management, including overcoming drug resistance and enhancing immunomodulation for vaccine therapy.
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