Literature DB >> 21827739

Green tea catechin, epigallocatechin-3-gallate (EGCG): mechanisms, perspectives and clinical applications.

Brahma N Singh1, Sharmila Shankar, Rakesh K Srivastava.   

Abstract

An expanding body of preclinical evidence suggests EGCG, the major catechin found in green tea (Camellia sinensis), has the potential to impact a variety of human diseases. Apparently, EGCG functions as a powerful antioxidant, preventing oxidative damage in healthy cells, but also as an antiangiogenic and antitumor agent and as a modulator of tumor cell response to chemotherapy. Much of the cancer chemopreventive properties of green tea are mediated by EGCG that induces apoptosis and promotes cell growth arrest by altering the expression of cell cycle regulatory proteins, activating killer caspases, and suppressing oncogenic transcription factors and pluripotency maintain factors. In vitro studies have demonstrated that EGCG blocks carcinogenesis by affecting a wide array of signal transduction pathways including JAK/STAT, MAPK, PI3K/AKT, Wnt and Notch. EGCG stimulates telomere fragmentation through inhibiting telomerase activity. Various clinical studies have revealed that treatment by EGCG inhibits tumor incidence and multiplicity in different organ sites such as liver, stomach, skin, lung, mammary gland and colon. Recent work demonstrated that EGCG reduced DNMTs, proteases, and DHFR activities, which would affect transcription of TSGs and protein synthesis. EGCG has great potential in cancer prevention because of its safety, low cost and bioavailability. In this review, we discuss its cancer preventive properties and its mechanism of action at numerous points regulating cancer cell growth, survival, angiogenesis and metastasis. Therefore, non-toxic natural agent could be useful either alone or in combination with conventional therapeutics for the prevention of tumor progression and/or treatment of human malignancies. Copyright Â
© 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21827739      PMCID: PMC4082721          DOI: 10.1016/j.bcp.2011.07.093

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  97 in total

1.  Epigenetic modulation of the retinoid X receptor alpha by green tea in the azoxymethane-Apc Min/+ mouse model of intestinal cancer.

Authors:  Suresh R Volate; Stephanie J Muga; Ala Y Issa; Daniela Nitcheva; Theresa Smith; Michael J Wargovich
Journal:  Mol Carcinog       Date:  2009-10       Impact factor: 4.784

2.  Angiogenesis as a therapeutic target in cancer.

Authors:  Gireesh Kumaran; Andrew R Clamp; Gordon C Jayson
Journal:  Clin Med (Lond)       Date:  2008-08       Impact factor: 2.659

3.  Green tea constituent (--)-epigallocatechin-3-gallate inhibits topoisomerase I activity in human colon carcinoma cells.

Authors:  S J Berger; S Gupta; C A Belfi; D M Gosky; H Mukhtar
Journal:  Biochem Biophys Res Commun       Date:  2001-10-19       Impact factor: 3.575

4.  Cancer-preventive effects of drinking green tea among a Japanese population.

Authors:  K Imai; K Suga; K Nakachi
Journal:  Prev Med       Date:  1997 Nov-Dec       Impact factor: 4.018

5.  Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: a preliminary report from a one-year proof-of-principle study.

Authors:  Saverio Bettuzzi; Maurizio Brausi; Federica Rizzi; Giovanni Castagnetti; Giancarlo Peracchia; Arnaldo Corti
Journal:  Cancer Res       Date:  2006-01-15       Impact factor: 12.701

6.  Green tea inhibits vascular endothelial growth factor (VEGF) induction in human breast cancer cells.

Authors:  Maryam R Sartippour; Zhi-Ming Shao; David Heber; Perrin Beatty; Liping Zhang; Canhui Liu; Lee Ellis; Wen Liu; Vay Liang Go; Mai N Brooks
Journal:  J Nutr       Date:  2002-08       Impact factor: 4.798

7.  FOXO transcription factors and VEGF neutralizing antibody enhance antiangiogenic effects of resveratrol.

Authors:  Rakesh K Srivastava; Terry G Unterman; Sharmila Shankar
Journal:  Mol Cell Biochem       Date:  2009-12-11       Impact factor: 3.396

8.  Role of p53 and NF-kappaB in epigallocatechin-3-gallate-induced apoptosis of LNCaP cells.

Authors:  Kedar Hastak; Sanjay Gupta; Nihal Ahmad; Mukesh K Agarwal; Munna L Agarwal; Hasan Mukhtar
Journal:  Oncogene       Date:  2003-07-31       Impact factor: 9.867

9.  A major constituent of green tea, EGCG, inhibits the growth of a human cervical cancer cell line, CaSki cells, through apoptosis, G(1) arrest, and regulation of gene expression.

Authors:  Woong Shick Ahn; Seung Won Huh; Su-Mi Bae; Insu P Lee; Jun Mo Lee; Sung Eun Namkoong; Chong Kook Kim; Jeong-Im Sin
Journal:  DNA Cell Biol       Date:  2003-03       Impact factor: 3.311

10.  Epigallocatechin gallate (EGCG) mimics insulin action on the transcription factor FOXO1a and elicits cellular responses in the presence and absence of insulin.

Authors:  Siobhan Anton; Laura Melville; Graham Rena
Journal:  Cell Signal       Date:  2006-07-25       Impact factor: 4.315

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  331 in total

1.  EGCG prevents PCB-126-induced endothelial cell inflammation via epigenetic modifications of NF-κB target genes in human endothelial cells.

Authors:  Dandan Liu; Jordan T Perkins; Bernhard Hennig
Journal:  J Nutr Biochem       Date:  2015-10-26       Impact factor: 6.048

2.  The anti-fibrotic effects of epigallocatechin-3-gallate in bile duct-ligated cholestatic rats and human hepatic stellate LX-2 cells are mediated by the PI3K/Akt/Smad pathway.

Authors:  Dong-ke Yu; Cai-xia Zhang; Shuang-shuang Zhao; Sheng-hua Zhang; Hao Zhang; Shi-ying Cai; Rong-guang Shao; Hong-wei He
Journal:  Acta Pharmacol Sin       Date:  2015-03-16       Impact factor: 6.150

3.  The Inhibitory Effect of Epigallocatechin Gallate on the Viability of T Lymphoblastic Leukemia Cells is Associated with Increase of Caspase-3 Level and Fas Expression.

Authors:  Masome Ghasemi-Pirbaluti; Batoul Pourgheysari; Hedayatollah Shirzad; Zahra Sourani; Pezhman Beshkar
Journal:  Indian J Hematol Blood Transfus       Date:  2017-08-01       Impact factor: 0.900

4.  Obesity treatment by epigallocatechin-3-gallate-regulated bile acid signaling and its enriched Akkermansia muciniphila.

Authors:  Lili Sheng; Prasant Kumar Jena; Hui-Xin Liu; Ying Hu; Nidhi Nagar; Denise N Bronner; Matthew L Settles; Andreas J Bäumler; Yu-Jui Yvonne Wan
Journal:  FASEB J       Date:  2018-06-08       Impact factor: 5.191

Review 5.  The organic anion transporter (OAT) family: a systems biology perspective.

Authors:  Sanjay K Nigam; Kevin T Bush; Gleb Martovetsky; Sun-Young Ahn; Henry C Liu; Erin Richard; Vibha Bhatnagar; Wei Wu
Journal:  Physiol Rev       Date:  2015-01       Impact factor: 37.312

6.  Cloning of a caffeoyl-coenzyme A O-methyltransferase from Camellia sinensis and analysis of its catalytic activity.

Authors:  Yue Zhang; Hai-peng Lv; Cheng-ying Ma; Li Guo; Jun-feng Tan; Qun-hua Peng; Zhi Lin
Journal:  J Zhejiang Univ Sci B       Date:  2015-02       Impact factor: 3.066

Review 7.  Modulation of Inflammatory Response to Implanted Biomaterials Using Natural Compounds.

Authors:  Maria Yanez; James Blanchette; Ehsan Jabbarzadeh
Journal:  Curr Pharm Des       Date:  2017       Impact factor: 3.116

8.  Medical perspective in testicular ischemia-reperfusion injury.

Authors:  Salvatore Arena; Roberta Iacona; Pietro Antonuccio; Tiziana Russo; Vincenzo Salvo; Eloisa Gitto; Pietro Impellizzeri; Carmelo Romeo
Journal:  Exp Ther Med       Date:  2017-03-30       Impact factor: 2.447

9.  Ambient Profiling of Phenolic Content in Tea Infusions by Matrix-Assisted Ionization in Vacuum.

Authors:  Robert B Cody
Journal:  J Am Soc Mass Spectrom       Date:  2018-05-29       Impact factor: 3.109

10.  Role of Ku70 and Bax in epigallocatechin-3-gallate-induced apoptosis of A549 cells in vivo.

Authors:  Jing-Jing Li; Qi-Hua Gu; Min Li; Hua-Ping Yang; Li-Ming Cao; Cheng-Ping Hu
Journal:  Oncol Lett       Date:  2012-10-16       Impact factor: 2.967

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