Abstract |
We have previously reported that epigallocatechin gallate (EGCG) strongly inhibits the in vitro phenol sulfotransferase (P-ST) activity of a human colon carcinoma cell line, Caco-2. In the present study, we examined the ability of EGCG to inhibit the sulfation of 1-naphthol in intact Caco-2 cells. Sulfation of 1-naphthol was detected in Caco-2 cells after 2 h of incubation, and was observed to continue for 24 h, resulting in an accumulation of sulfated 1-naphthol. Sulfation was strongly inhibited by the addition of EGCG to the culture medium. The IC50 of EGCG was calculated to be 20 microM; this value is similar to that obtained from in vitro assays (14 microM) [Ref. Tamura et al., Biol. Pharm. Bull., 23, 695, (2000)]. These results indicate that catechins are capable of inhibiting P-ST activity in intact cells as well as in vitro. We believe that the inhibitory activity of catechins might be the mechanism by which catechins (and green tea) exert anti-carcinogenic activity against procarcinogenic compounds that require P-ST activation in vivo.
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Authors | T Isozaki, H Tamura |
Journal | Biological & pharmaceutical bulletin
(Biol Pharm Bull)
Vol. 24
Issue 9
Pg. 1076-8
(Sep 2001)
ISSN: 0918-6158 [Print] Japan |
PMID | 11558573
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Enzyme Inhibitors
- Naphthols
- Sulfates
- 1-naphthol
- Catechin
- epigallocatechin gallate
- Arylsulfotransferase
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Topics |
- Antineoplastic Agents
(pharmacology)
- Arylsulfotransferase
(antagonists & inhibitors)
- Caco-2 Cells
- Catechin
(analogs & derivatives, pharmacology)
- Chromatography, High Pressure Liquid
- Depression, Chemical
- Enzyme Inhibitors
(pharmacology)
- Humans
- Naphthols
(metabolism)
- Sulfates
(metabolism)
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