Tea polyphenols for health promotion

被引:987
作者
Khan, Naghma [1 ]
Mukhtar, Hasan [1 ]
机构
[1] Univ Wisconsin, Dept Dermatol, Med Sci Ctr, Madison, WI 53706 USA
关键词
cancer prevention; health effects; medicinal properties; tea polyphenols;
D O I
10.1016/j.lfs.2007.06.011
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
People have been consuming brewed tea from the leaves of the Camellia sinensis plant for almost 50 centuries. Although health benefits have been attributed to tea, especially green tea consumption since the beginning of its history, scientific investigations of this beverage and its constituents have been underway for less than three decades. Currently, tea, in the form of green or black tea, next to water, is the most widely consumed beverage in the world. In vitro and animal studies provide strong evidence that polyphenols derived from tea may possess the bioactivity to affect the pathogenesis of several chronic diseases. Among all tea polyphenols, epigallocatecbin-3-gallate has been shown to be responsible for much of the health promoting ability of green tea. Tea and tea preparations have been shown to inhibit tumorigenesis in a variety of animal models of carcinogenesis. However, with increasing interest in the health promoting properties of tea and a significant rise in scientific investigation, this review covers recent findings on the medicinal properties and health benefits of tea with special reference to cancer and cardiovascular diseases. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:519 / 533
页数:15
相关论文
共 128 条
[1]   Combined inhibitory effects of green tea polyphenols and selective cyclooxygenase-2 inhibitors on the growth of human prostate cancer cells both in vitro and in vivo [J].
Adhami, Vaqar Mustafa ;
Malik, Arshi ;
Zaman, Najia ;
Sarfaraz, Sami ;
Siddiqui, Imtiaz Ahmad ;
Syed, Deeba Nadeem ;
Afaq, Farrukh ;
Pasha, Farrukh Sierre ;
Saleem, Mohammad ;
Mukhtar, Hasan .
CLINICAL CANCER RESEARCH, 2007, 13 (05) :1611-1619
[2]   Insulin-like growth factor-I axis as a pathway for cancer chemoprevention [J].
Adhami, Vaqar Mustafa ;
Afaq, Farrukh ;
Mukhtar, Hasan .
CLINICAL CANCER RESEARCH, 2006, 12 (19) :5611-5614
[3]   Oral consumption of green tea polyphenols inhibits insulin-like growth factor-i-induced signaling in an autochthonous mouse model of prostate cancer [J].
Adhami, VM ;
Siddiqui, IA ;
Ahmad, N ;
Gupta, S ;
Mukhtar, H .
CANCER RESEARCH, 2004, 64 (23) :8715-8722
[4]   Molecular targets for green tea in prostate cancer prevention [J].
Adhami, VM ;
Ahmad, N ;
Mukhtar, H .
JOURNAL OF NUTRITION, 2003, 133 (07) :2417S-2424S
[5]   Suppression of UVB-induced phosphorylation of mitogen-activated protein kinases and nuclear factor kappa B by green tea polyphenol in SKH-1 hairless mice [J].
Afaq, F ;
Ahmad, N ;
Mukhtar, H .
ONCOGENE, 2003, 22 (58) :9254-9264
[6]   Potential therapeutic applications of tea in dermatology [J].
Alexis, AF ;
Jones, VA ;
Stiller, MJ .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1999, 38 (10) :735-743
[7]   Growth inhibitory and antimetastatic effect of green tea polyphenols on metastasis-specific mouse mammary carcinoma 4T1 cells in vitro and in vivo systems (Publication with Expression of Concern. See vol. 24, pg. 6103, 2018) [J].
Baliga, MS ;
Meleth, S ;
Kadiyar, SK .
CLINICAL CANCER RESEARCH, 2005, 11 (05) :1918-1927
[8]   In vitro and in vivo antimicrobial action of tea:: The commonest beverage of Asia [J].
Bandyopadhyay, D ;
Chatterjee, TK ;
Dasgupta, A ;
Lourduraja, J ;
Dastidar, SG .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2005, 28 (11) :2125-2127
[9]   Black tea polyphenols suppress cell proliferation and induce apoptosis during benzo(a)pyrene-induced lung carcinogenesis [J].
Banerjee, S ;
Manna, S ;
Saha, P ;
Panda, CK ;
Das, S .
EUROPEAN JOURNAL OF CANCER PREVENTION, 2005, 14 (03) :215-221
[10]   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 [J].
Bettuzzi, S ;
Brausi, M ;
Rizzi, F ;
Castagnetti, G ;
Peracchia, G ;
Corti, A .
CANCER RESEARCH, 2006, 66 (02) :1234-1240