Literature DB >> 12433185

Cancer chemoprevention by tea polyphenols through modulating signal transduction pathways.

Jen-Kun Lin1.   

Abstract

The action mechanisms of several chemopreventive agents derived from herbal medicine and edible plants have become attractive issues in cancer research. Tea is the most widely consumed beverage worldwide. Recently, the cancer chemopreventive actions of tea have been intensively investigated. It have been demonstrated that the active principles of tea were attributed to their tea polyphenols. Recently, tremendous progress has been made in elucidating the molecular mechanisms of cancer chemoprevention by tea and tea polyphenols. The suppression of various tumor biomarkers including growth factor receptor tyrosine kinases, cytokine receptor kinases, PI3K, phosphatases, ras, raf, MAPK cascades, N x FB, I x B kinase, PKA, PKB, PKC, c-jun, c-fos, c-myc, cdks, cyclins, and related transducing proteins by tea polyphenols has been studied in our laboratory and others. The I x B kinase (IKK) activity in LPS-activated murine macrophages (RAW 264.7 cells) was found to be inhibited by various tea polyphenols including (-) epigallocatechin-3-gallate (EGCG), theaflavin (TF-1), theaflavin-3-gallate (TF-2) and theaflavin-3,3'-digallate (TF-3). TF-3 inhibited IKK activity in activated macrophages more strongly than did the other tea polyphenols. TF-3 inhibited both IKK1 and IKK2 activity and prevented the degradation of I x B x and I x B x in activated macrophage cells. The results suggested that the inhibition of IKK activity by TF-3 and other tea polyphenols could occur by a direct effect on IKKs or on upstream events in the signal transduction pathway. TF-3 and other tea polyphenols blocked phosphorylation of IB from the cytosolic fraction, inhibited NFB activity and inhibited increases in inducible nitric oxide synthase levels in activated macrophage. TF-3 and other tea polyphenols also inhibited strongly the activities of xanthine oxidase, cyclooxygenase, EGF-receptor tyrosine kinase and protein kinase C. These results suggest that TF-3 and other tea polyphenols may exert their cancer chemoprevention through suppressing tumor promotion and inflammation by blocking signal transduction. The mechanisms of this inhibition may be due to the blockade of the mitogenic and differentiating signals through modulating EGFR function, MAPK cascades, NFkappaB activation as well as c-myc, c-jun and c-fos expression.

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Year:  2002        PMID: 12433185     DOI: 10.1007/bf02976924

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  26 in total

1.  Black tea polyphenol theaflavin suppresses LPS-induced ICAM-1 and VCAM-1 expression via blockage of NF-κB and JNK activation in intestinal epithelial cells.

Authors:  Young-A Song; Young-Lan Park; Sun-Hye Yoon; Kyu-Yeol Kim; Sung-Bum Cho; Wan-Sik Lee; Ik-Joo Chung; Young-Eun Joo
Journal:  Inflamm Res       Date:  2010-12-24       Impact factor: 4.575

Review 2.  Mitochondria-Centric Review of Polyphenol Bioactivity in Cancer Models.

Authors:  Jan F Stevens; Johana S Revel; Claudia S Maier
Journal:  Antioxid Redox Signal       Date:  2017-12-11       Impact factor: 8.401

3.  Fbxl18 targets LRRK2 for proteasomal degradation and attenuates cell toxicity.

Authors:  Xiaodong Ding; Sandeep K Barodia; Lisha Ma; Matthew S Goldberg
Journal:  Neurobiol Dis       Date:  2016-11-24       Impact factor: 5.996

4.  Synthesis of Naturally Occurring Tropones and Tropolones.

Authors:  Na Liu; Wangze Song; Casi M Schienebeck; Min Zhang; Weiping Tang
Journal:  Tetrahedron       Date:  2014-12-09       Impact factor: 2.457

5.  Cytotoxicity of epigallocatechin-3-gallate to LNCaP cells in the presence of Cu2+.

Authors:  Hai-ning Yu; Sheng-rong Shen; Yao-kang Xiong
Journal:  J Zhejiang Univ Sci B       Date:  2005-02       Impact factor: 3.066

6.  Phase I trial of daily oral Polyphenon E in patients with asymptomatic Rai stage 0 to II chronic lymphocytic leukemia.

Authors:  Tait D Shanafelt; Tim G Call; Clive S Zent; Betsy LaPlant; Deborah A Bowen; Michelle Roos; Charla R Secreto; Asish K Ghosh; Brian F Kabat; Mao-Jung Lee; Chung S Yang; Diane F Jelinek; Charles Erlichman; Neil E Kay
Journal:  J Clin Oncol       Date:  2009-05-26       Impact factor: 44.544

7.  Tea consumption and risk of breast cancer.

Authors:  Nagi Kumar; Linda Titus-Ernstoff; Polly A Newcomb; Amy Trentham-Dietz; Gabriella Anic; Kathleen M Egan
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-01       Impact factor: 4.254

8.  Diallyl disulfide-induced G2/M arrest of human gastric cancer MGC803 cells involves activation of p38 MAP kinase pathways.

Authors:  Jing-Ping Yuan; Gui-Hua Wang; Hui Ling; Qi Su; Yue-Hong Yang; Ying Song; Rong-Jun Tang; Yao Liu; Chen Huang
Journal:  World J Gastroenterol       Date:  2004-09-15       Impact factor: 5.742

9.  The green tea component EGCG inhibits RNA polymerase III transcription.

Authors:  Joby Jacob; Stephanie Cabarcas; Ingrid Veras; Nurulain Zaveri; Laura Schramm
Journal:  Biochem Biophys Res Commun       Date:  2007-07-02       Impact factor: 3.575

10.  Pre- and post-initiation modulating effects of green tea ingestion on rat hepatocarcinogenesis.

Authors:  Hyung-Sook Kim; Hee-Seon Kim; Haymie Choi
Journal:  Nutr Res Pract       Date:  2008-12-30       Impact factor: 1.926

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