GREEN TEA EPIGALLOCATECHIN GALLATE SHOWS A PRONOUNCED GROWTH-INHIBITORY EFFECT ON CANCEROUS CELLS BUT NOT ON THEIR NORMAL COUNTERPARTS

Citation
Zp. Chen et al., GREEN TEA EPIGALLOCATECHIN GALLATE SHOWS A PRONOUNCED GROWTH-INHIBITORY EFFECT ON CANCEROUS CELLS BUT NOT ON THEIR NORMAL COUNTERPARTS, Cancer letters, 129(2), 1998, pp. 173-179
Citations number
19
Categorie Soggetti
Oncology
Journal title
ISSN journal
03043835
Volume
129
Issue
2
Year of publication
1998
Pages
173 - 179
Database
ISI
SICI code
0304-3835(1998)129:2<173:GTEGSA>2.0.ZU;2-Z
Abstract
(-)-Epigallocatechin gallate (EGCG), a catechin polyphenol compound, r epresents the main ingredient of green tea extract. Although EGCG has been shown to be growth inhibitory in a number of tumor cell Lines, it is not clear whether the effect is cancer-specific. In this study we compared the effect of EGCG on the growth of SV40 virally transformed WI38 human fibroblasts (WI38VA) with that of normal WI38 cells. The IC 50 value of EGCG was estimated to be 120 and 10 mu M for WI38 and WI38 VA cells, respectively. Thus, EGCG at 40 mu M completely inhibited the growth of WI38VA cells, but had little or no inhibitory effect on the growth of WI38 cells. Similar differential growth inhibition was also observed between a human colorectal cancer cell line (Caco-2), a brea st cancer cell line (Hs578T) and their respective normal counterparts. EGCG at a concentration range of 40-200 mu M induced a significant am ount of apoptosis in WI38VA cultures, but not in WI38 cultures, as det ermined by terminal deoxynucleotidyl transferase assay. After exposure to EGCG at 200 mu M for 8 h, more than 50% of WI38VA cells in a confl uent culture became apoptotic. In contrast, less than 1% of WI38 cells displayed apoptotic labeling under the same condition. EGCG did not a ffect the serum-induced expression of c-fos and c-myc genes in normal WI38 cells. However, it significantly enhanced their expression in tra nsformed WI38VA cells. It is possible that differential modulation of certain genes, such as c-fos and c-myc, may cause differential effects of EGCG on the growth and death of cancer cells. (C) 1998 Published b y Elsevier Science Ireland Ltd. All rights reserved.