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      Tea Polyphenol Intake and Changes in Serum Pepsinogen Levels

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          Abstract

          Following a phase I study, a phase II study was conducted to evaluate the effects of two different doses of tea polyphenols on serum pepsinogen levels. Subjects were patients aged 40 to 69 years who had undergone gastroscopy between 1995 and 1997 at Aichi Cancer Center Hospital, and had been found to have no disease requiring medication. Those with pepsinogen I <70 ng/ml and pepsinogen I/II ratio ?6 were included in this study. Capsules containing 100 mg of tea polyphenols were administered for 1 year: 1 capsule per day for 101 patients (42 males and 59 females), and 6 capsules (equivalent to 10 cups) per day for 83 patients (30 males and 53 females). The enrollment of the 1 capsule group preceded that of the 6 capsule group, in which re‐participation was allowed. Blood samples were obtained 1 year after participation from 86 participants of the 1 capsule group and 77 participants (43 new participants and 34 re‐participants) of the 6 capsule group. The compliance in polyphenol capsule intake ranged from 11.4 to 105.7% (87.6% on average) of the scheduled amount for the 1 capsule group and 3.2 to 112.3% (77.8% on average) for the 6 capsule group. No serious polyphenol‐related adverse effects were reported. The difference in pepsinogen I between before and after 1 year intake of the polyphenol was 3.1 ng/ml for the 43 participants of the 6 capsule group, but 3.5 ng/ml for the 1 capsule group. The mean pepsinogen I/II ratio for the 43 participants increased from 2.37 by 0.08. This increase was not larger than that for the 1 capsule group (from 2.61 by 0.11). Among 34 participants in both interventions, no significant increase in pepsinogen I and I/II ratio for the 6 capsule intervention was observed. This result suggests that additional polyphenol intake for 1 year in Japanese does not improve pepsinogen levels, which are considered to reflect stomach atrophy, a high‐risk condition for stomach cancer.

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          Nutrition Intervention Trials in Linxian, China: Supplementation With Specific Vitamin/Mineral Combinations, Cancer Incidence, and Disease-Specific Mortality in the General Population

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            Inhibition of growth and induction of apoptosis in human cancer cell lines by tea polyphenols.

            In order to study the biological activities of tea preparations and purified tea polyphenols, their growth inhibitory effects were investigated using four human cancer cell lines. Growth inhibition was measured by [3H]thymidine incorporation after 48 h of treatment. The green tea catechins (-)-epigallocatechin-3-gallate (EGCG) and (-)-epigallocatechin (EGC) displayed strong growth inhibitory effects against lung tumor cell lines H661 and H1299, with estimated IC50 values of 22 microM, but were less effective against lung cancer cell line H441 and colon cancer cell line HT-29 with IC50 values 2- to 3-fold higher. (-)-Epicatechin-3-gallate, had lower activities, and (-)-epicatechin was even less effective. Preparations of green tea polyphenols and theaflavins had higher activities than extracts of green tea and decaffeinated green tea. The results suggest that the growth inhibitory activity of tea extracts is caused by the activities of different tea polyphenols. Exposure of H661 cells to 30 microM EGCG, EGC or theaflavins for 24 h led to the induction of apoptosis as determined by an annexin V apoptosis assay, showing apoptosis indices of 23, 26 and 8%, respectively; with 100 microM of these compounds, the apoptosis indices were 82, 76 and 78%, respectively. Incubation of H661 cells with EGCG also induced a dose-dependent formation of H2O2. Addition of H2O2 to H661 cells caused apoptosis in a manner similar to that caused by EGCG. The EGCG-induced apoptosis in H661 cells was completely inhibited by exogenously added catalase (50 units/ml). These results suggest that tea polyphenol-induced production of H2O2 may mediate apoptosis and that this may contribute to the growth inhibitory activities of tea polyphenols in vitro.
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              Why drinking green tea could prevent cancer.

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                Author and article information

                Journal
                Jpn J Cancer Res
                Jpn. J. Cancer Res
                10.1111/(ISSN)1349-7006a
                CAS
                Japanese Journal of Cancer Research : Gann
                Blackwell Publishing Ltd (Oxford, UK )
                0910-5050
                1876-4673
                February 1999
                : 90
                : 2 ( doiID: 10.1111/cas.1999.90.issue-2 )
                : 136-143
                Affiliations
                [ 1 ]Division of Epidemiology, Aichi Cancer Center Hospital, 1–1 Kanokoden, Chikusa‐ku, Nagoya 464–8681
                [ 2 ]Aichi Cancer Center Research Institute, Aichi Cancer Center Hospital, 1–1 Kanokoden, Chikusa‐ku, Nagoya 464–8681
                [ 3 ]Department of Gastroenterology, Aichi Cancer Center Hospital, 1–1 Kanokoden, Chikusa‐ku, Nagoya 464–8681
                [ 4 ]Department of Clinical Laboratory, General Health Center, 3–2‐1 Samnomaru, Naka‐ku, Nagoya 460–0001
                [ 5 ]Department of Clinical Laboratory, Aichi Cancer Center Hospital, 1–1 Kanokoden, Chikusa‐ku, Nagoya 464–8681
                Author notes
                Article
                CAE136
                10.1111/j.1349-7006.1999.tb00726.x
                5926041
                10189883
                2777b743-6656-4091-b91f-5278c82c5609
                History
                Page count
                References: 29, Pages: 8
                Categories
                Article
                Custom metadata
                2.0
                February 1999
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.6.9 mode:remove_FC converted:04.11.2015

                tea polyphenols,pepsinogens,adverse effects,phase ii trial

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