Green tea constituent (--)-epigallocatechin-3-gallate inhibits topoisomerase I activity in human colon carcinoma cells
- PMID: 11594758
- DOI: 10.1006/bbrc.2001.5736
Green tea constituent (--)-epigallocatechin-3-gallate inhibits topoisomerase I activity in human colon carcinoma cells
Abstract
DNA topoisomerases I and II are essential for cell survival and play critical roles in DNA metabolism and structure. Inhibitors of topoisomerase constitute a novel family of antitumor agents with demonstrated clinical activity in human malignancies. The clinical use of these agents is limited due to severe toxic effects on normal cells. Therefore, there is a need to develop novel, nontoxic topoisomerase inhibitors that have the ability to spare normal cells. Recent studies have shown that green tea and its major polyphenolic constituent, epigallocatechin-3-gallate (EGCG), impart growth inhibitory responses to cancer cells but not to normal cells. Based on the knowledge that EGCG induces DNA damage, cell cycle arrest, and apoptosis, we considered the possibility of the involvement of topoisomerase in the antiproliferative response of EGCG. Here, for the first time, we show that EGCG inhibits topoisomerase I, but not topoisomerase II in several human colon carcinoma cell lines. Based on this study it is tempting to suggest that combination of EGCG with other conventional topoisomerase inhibitors could be an improved strategy for treatment of colon cancer. The possible role of EGCG as a chemotherapeutic agent needs to be investigated.
Copyright 2001 Academic Press.
Similar articles
-
Growth inhibition, cell-cycle dysregulation, and induction of apoptosis by green tea constituent (-)-epigallocatechin-3-gallate in androgen-sensitive and androgen-insensitive human prostate carcinoma cells.Toxicol Appl Pharmacol. 2000 Apr 1;164(1):82-90. doi: 10.1006/taap.1999.8885. Toxicol Appl Pharmacol. 2000. PMID: 10739747
-
EGCG, a major component of green tea, inhibits tumour growth by inhibiting VEGF induction in human colon carcinoma cells.Br J Cancer. 2001 Mar 23;84(6):844-50. doi: 10.1054/bjoc.2000.1691. Br J Cancer. 2001. PMID: 11259102 Free PMC article.
-
Green tea polyphenols and its constituent epigallocatechin gallate inhibits proliferation of human breast cancer cells in vitro and in vivo.Cancer Lett. 2007 Jan 8;245(1-2):232-41. doi: 10.1016/j.canlet.2006.01.027. Epub 2006 Mar 6. Cancer Lett. 2007. PMID: 16519995
-
Role of epigallocatechin gallate (EGCG) in the treatment of breast and prostate cancer.Life Sci. 2006 Nov 17;79(25):2329-36. doi: 10.1016/j.lfs.2006.07.036. Epub 2006 Aug 5. Life Sci. 2006. PMID: 16945390 Review.
-
New cancer treatment strategy using combination of green tea catechins and anticancer drugs.Cancer Sci. 2011 Feb;102(2):317-23. doi: 10.1111/j.1349-7006.2010.01805.x. Epub 2010 Dec 30. Cancer Sci. 2011. PMID: 21199169 Review.
Cited by
-
Progress in nanotechnology based approaches to enhance the potential of chemopreventive agents.Cancers (Basel). 2011 Jan 21;3(1):428-45. doi: 10.3390/cancers3010428. Cancers (Basel). 2011. PMID: 24212623 Free PMC article.
-
Emerging Therapeutic Potential of SIRT6 Modulators.J Med Chem. 2021 Jul 22;64(14):9732-9758. doi: 10.1021/acs.jmedchem.1c00601. Epub 2021 Jul 2. J Med Chem. 2021. PMID: 34213345 Free PMC article. Review.
-
Epigenetic marvels: exploring the landscape of colorectal cancer treatment through cutting-edge epigenetic-based drug strategies.Clin Epigenetics. 2025 Feb 22;17(1):34. doi: 10.1186/s13148-025-01844-w. Clin Epigenetics. 2025. PMID: 39987205 Free PMC article. Review.
-
An Association Map on the Effect of Flavonoids on the Signaling Pathways in Colorectal Cancer.Int J Med Sci. 2016 Apr 29;13(5):374-85. doi: 10.7150/ijms.14485. eCollection 2016. Int J Med Sci. 2016. PMID: 27226778 Free PMC article. Review.
-
Epigallocatechin-3-gallate Can Prevent Type 2 Human Papillomavirus E7 from Suppressing Interferon-Stimulated Genes.Int J Mol Sci. 2021 Feb 28;22(5):2418. doi: 10.3390/ijms22052418. Int J Mol Sci. 2021. PMID: 33670861 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources