GSTM1, GSTT1, GSTP1, and GSTA1 polymorphisms and urinary isothiocyanate metabolites following broccoli consumption in humans

被引:40
作者
Steck, Susan E. [1 ]
Gammon, Marilie D.
Hebert, James R.
Wall, Denise E.
Zeisel, Steven H.
机构
[1] Univ S Carolina, Arnold Sch Publ Hlth, Dept Epidemiol & Biostat, Columbia, SC 29208 USA
[2] S Carolina Statewide Canc Prevent & Control Progr, Columbia, SC 29208 USA
[3] Univ N Carolina, Sch Publ Hlth, Dept Epidemiol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Sch Publ Hlth, Dept Nutr, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Sch Med, Dept Nutr, Chapel Hill, NC 27599 USA
关键词
D O I
10.1093/jn/137.4.904
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Isothiocyanates (ITC) are potentially anticarcinogenic phytochemicals formed from the metabolism of glucosinolates and are found in cruciferous vegetables as well as a select number of other foods. ITC are both substrates for and inducers of glutathione S-transferase (GST) phase 11 metabolizing enzymes involved in carcinogen detoxification as well as effectors of phase I pathways. Previous studies report mixed results on the interaction between cruciferous vegetable intake, GST polymorphisms, and risk of cancer. We conducted a study of 114 healthy human subjects between 18 and 50 y of age to examine the biologic mechanism underlying the associations, specifically, to assess whether GST genotype is associated with urinary ITC metabolites following a known dose of broccoli. After 48 h of abstaining from all sources of glucosinolates, participants provided a blood sample, consumed 1 meal containing 2.5 g broccoli/kg body weight, and collected urine for 24 h. ITC metabolites were measured in the urine using a HPLC cyclocondensation assay. DNA was extracted from blood samples, and GSTM1 deletion, GSTT1 deletion, GSTP7 Ile705Val, and GSTA1*A/*B were genotyped by matrix-assisted laser desorption/ionization time-of-flight. A chi-square test was used to compare high and low ITC excretion levels across genotypes. ITC levels were regressed on genotype, adjusting for gender. There were no substantial differences in ITC levels among genotypes, either individually or in combination. Contrary to our hypothesis, a higher proportion of GSTM1 null individuals had high ITC excretion (62%) compared with the proportion of GSTM1 present with high ITC excretion (39%) (P = 0.03). These results are in agreement with another feeding study, and lend support to the idea of alternative routes of ITC metabolism.
引用
收藏
页码:904 / 909
页数:6
相关论文
共 40 条
[1]   Effects of glutathione S-transferase A1 (GSTA1) genotype and potential modifiers on breast cancer risk [J].
Ahn, Jiyoung ;
Gammon, Marilie D. ;
Santella, Regina M. ;
Gaudet, Mia M. ;
Britton, Julie A. ;
Teitelbaum, Susan L. ;
Terry, Mary Beth ;
Neugut, Alfred I. ;
Eng, Sybil M. ;
Zhang, Yuesheng ;
Garza, Cutberto ;
Ambrosone, Christine B. .
CARCINOGENESIS, 2006, 27 (09) :1876-1882
[2]   Breast cancer risk in premenopausal women is inversely associated with consumption of broccoli, a source of isothiocyanates, but is not modified by GST genotype [J].
Ambrosone, CB ;
McCann, SE ;
Freudenheim, JL ;
Marshall, JR ;
Zhang, YS ;
Shields, PG .
JOURNAL OF NUTRITION, 2004, 134 (05) :1134-1138
[3]   Effect of cruciferous vegetables on lung cancer in patients stratified by genetic status: a mendelian randomisation approach [J].
Brennan, P ;
Hsu, CC ;
Moullan, N ;
Szeszenia-Dabrowska, N ;
Lissowska, J ;
Zaridze, D ;
Rudnai, P ;
Fabianova, E ;
Mates, D ;
Bencko, V ;
Foretova, L ;
Janout, V ;
Gemignani, F ;
Chabrier, A ;
Hall, J ;
Hung, RJ ;
Boffetta, P ;
Canzian, F .
LANCET, 2005, 366 (9496) :1558-1560
[4]   Effect of polymorphism in the human glutathione S-transferase A1 promoter on hepatic GSTA1 and GSTA2 expression [J].
Coles, BF ;
Morel, F ;
Rauch, C ;
Huber, WW ;
Yang, M ;
Teitel, CH ;
Green, B ;
Lang, NP ;
Kadlubar, FF .
PHARMACOGENETICS, 2001, 11 (08) :663-669
[5]  
Fowke JH, 2003, CANCER EPIDEM BIOMAR, V12, P1536
[6]  
Fowke JH, 2003, CANCER RES, V63, P3980
[7]   Using isothiocyanate excretion as a biological marker of Brassica vegetable consumption in epidemiological studies:: evaluating the sources of variability [J].
Fowke, JH ;
Fahey, JW ;
Stephenson, KK ;
Hebert, JR .
PUBLIC HEALTH NUTRITION, 2001, 4 (03) :837-846
[8]  
Garte S, 2001, CANCER EPIDEM BIOMAR, V10, P1239
[9]   Glutathione S-transferase M1 polymorphism and metabolism of sulforaphane from standard and high-glucosinolate broccoli [J].
Gasper, AV ;
Al-janobi, A ;
Smith, JA ;
Bacon, JR ;
Fortun, P ;
Atherton, C ;
Taylor, MA ;
Hawkey, CJ ;
Barrett, DA ;
Mithen, RF .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2005, 82 (06) :1283-1291
[10]   Diet, GSTM1 and GSTT1 and head and neck cancer [J].
Gaudet, MM ;
Olshan, AF ;
Poole, C ;
Weissler, MC ;
Watson, M ;
Bell, DA .
CARCINOGENESIS, 2004, 25 (05) :735-740