Tea consumption, apoptosis, and colorectal adenomas

被引:4
作者
Il'yasova, D
Hodgson, ME
Martin, C
Galanko, J
Sandler, RS
机构
[1] Wake Forest Univ, Sch Med, Dept Epidemiol, Winston Salem, NC 27157 USA
[2] Univ N Carolina, Sch Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[3] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC USA
[4] Univ N Carolina, Sch Med, Ctr Gastrointestinal Biol & Dis, Chapel Hill, NC USA
关键词
adenoma; apoptosis; epidemiology; tea;
D O I
10.1097/00008469-200310000-00016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Induction of apoptosis has been suggested as a mechanism for the anti-carcinogenic effect of tea constituents in animals and in vitro studies. We addressed this hypothesis in a human study. Study participants were consecutive patients who underwent colonoscopy at the UNC Hospitals (August 1998 to March 2000). Biopsies were taken from normal rectal mucosa. Apoptosis was scored by the terminal deoxyribonucleotide transferase-mediated digoxigenin dUTP nick end labeling (TUNEL) method and by standard morphological criteria. The analysis included 171 patients with adenomas (cases) and 323 adenoma-free controls. After adjusting for sex, age, race, and BMI, apoptotic score was inversely associated with adenoma: the odds ratios (ORs) for linear trend associated with tertiles were 0.3 (0.3-0.5) for morphologic score and 0.5 (0.4-0.6) for the TUNEL score, respectively. Tea consumption (2-3 and > 3 versus < 2 servings/day) showed a weak negative association with adenoma: the ORs were 0.7 (0.3-1.4) and 0.5 (0.2-1.1), respectively. Neither measurement of apoptotic score changed by the level of tea consumption (P value for Kruskal-Wallis test greater than or equal to 0.5). We did not find statistical interaction between apoptotic score and tea consumption. Tea exposure is not associated with apoptosis in normal rectal tissue in vivo. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:439 / 443
页数:5
相关论文
共 54 条
  • [1] The chemistry of tea flavonoids
    Balentine, DA
    Wiseman, SA
    Bouwens, LCM
    [J]. CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) : 693 - 704
  • [2] BARON JA, 1994, CANCER EPIDEM BIOMAR, V3, P565
  • [3] Baron JA, 1997, CANCER EPIDEM BIOMAR, V6, P7
  • [4] BEDI A, 1995, CANCER RES, V55, P1811
  • [5] A DATA-BASED APPROACH TO DIET QUESTIONNAIRE DESIGN AND TESTING
    BLOCK, G
    HARTMAN, AM
    DRESSER, CM
    CARROLL, MD
    GANNON, J
    GARDNER, L
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 1986, 124 (03) : 453 - 469
  • [6] VALIDATION OF A SELF-ADMINISTERED DIET HISTORY QUESTIONNAIRE USING MULTIPLE DIET RECORDS
    BLOCK, G
    WOODS, M
    POTOSKY, A
    CLIFFORD, C
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 1990, 43 (12) : 1327 - 1335
  • [7] Effects of black tea, green tea and wine extracts on intestinal carcinogenesis induced by azoxymethane in F344 rats
    Caderni, G
    De Filippo, C
    Luceri, C
    Salvadori, M
    Giannini, A
    Biggeri, A
    Remy, S
    Cheynier, V
    Dolara, P
    [J]. CARCINOGENESIS, 2000, 21 (11) : 1965 - 1969
  • [8] Cerhan JR, 2001, NUTR CANCER, V41, P33, DOI 10.1207/S15327914NC41-1&amp
  • [9] 2_4
  • [10] Green tea epigallocatechin gallate shows a pronounced growth inhibitory effect on cancerous cells but not on their normal counterparts
    Chen, ZP
    Schell, JB
    Ho, CT
    Chen, KY
    [J]. CANCER LETTERS, 1998, 129 (02) : 173 - 179