Green tea catechins and vitamin e inhibit angiogenesis of human microvascular endothelial cells through suppression of il-8 production.

Epidemiological and animal studies have indicated that consumption of green tea and high vitamin E intake are associated with a reduced risk of developing certain forms of cancer. However, the inhibitory mechanism of green tea catechins and vitamin E in angiogenesis, an important process in tumor gr...

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Detalles Bibliográficos
Publicado en:Nutrition & Cancer Vol. 41; no. 1/2; pp. 119 - 126
Autores principales: Tang F, Meydani M
Formato: Journal Article
Publicado: Taylor & Francis Ltd 2001
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Epidemiological and animal studies have indicated that consumption of green tea and high vitamin E intake are associated with a reduced risk of developing certain forms of cancer. However, the inhibitory mechanism of green tea catechins and vitamin E in angiogenesis, an important process in tumor growth, has not been well established. In the present study, [alpha]-tocopherol and several major catechins of green tea (catechin, epicatechin, epicatechin gallate, epigallocatechin, and epigallocatechin gallate) were tested for their ability to inhibit tube formation in vitro using a model in which human microvascular endothelial cells were exposed to a constant rate of a physiologically low level of H[sub 2]O[sub 2]. In this model, the production of interleukin (IL)-8 by human microvascular endothelial cells at a low level of H[sub 2]O[sub 2] was required for angiogenesis, as assessed by tube formation in three-dimensional gel in culture. Vitamin E (d-[alpha]-tocopherol, 40 [mu]M) in the culture media significantly reduced IL-8 production and angiogenesis. Among the green tea catechins, epigallocatechin (0.5-1 [mu]M) was the most effective in reducing IL-8 production and inhibiting angiogenesis. These results suggest that consumption of green tea catechins or supplemental intake of vitamin E may have preventive effects on tumor development, mediated, at least in part, through inhibition of angiogenesis via suppression of IL-8 production.