Cruciferae interact with the UGT1A1*28 polymorphism to determine serum bilirubin levels in humans

被引:23
作者
Peterson, S
Bigler, J
Horner, NK
Potter, JD
Lampe, JW [1 ]
机构
[1] Univ Washington, Dept Epidemiol, Interdisciplinary Grad Program Nutr Sci, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
UGT1A1; polymorphism; chemoprevention; Cruciferae; bilirubin;
D O I
10.1093/jn/135.5.1051
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
UDP-glucuronosyltransferase (UGT) 1A1 is a conjugating biotransformation enzyme that plays a role in maintaining levels of endogenous compounds (e.g., bilirubin) and handling exogenous compounds, including carcinogens. The UGT1A1*28 polymorphism results in decreased UGT1A1 promoter activity due to 7 thymineadenine (TA) repeats instead of the commonly found 6 repeats. Studies indicate that foods from the botanical families Cruciferae (e.g., broccoli), Rutaceae (citrus), Liliaceae (e.g., onions), and Leguminosae (legumes) may increase UGT activity. We investigated, in an observational study, whether foods from these botanical groups were associated with increased UGT1A1 activity as indicated by serum bilirubin concentrations and whether the effect varied by UGT1A1*28 genotype, comparing those homozygous for the [TA](7)-repeat allele (7/7) to homozygous wild-types (6/6) and heterozygotes (6/7) combined. Healthy volunteers completed 3-d food records. Blood samples were drawn for genomic DNA collection and bilirubin measures. For total, direct, and indirect bilirubin measures, there was no significant association with any botanical group independently. There was a significant inverse association between all 3 bilirubin measures and interaction of UGT1A1*28 genotype with Cruciferae intake (P < 0.02 for each measure); individuals with the 7/7 genotype had reduced bilirubin concentrations with increased intake of cruciferous vegetables, whereas individuals with the 6/6 or 6/7 genotype did not. With regard to UGT1A1-conjugated carcinogens (e.g., heterocyclic amines, polycyclic aromatic hydrocarbons), individuals with decreased UGT1A1 activity due to the 7/7 genotype may be at greater risk for carcinogenesis, but our results imply that they also may have greater opportunity to decrease that risk through dietary intervention.
引用
收藏
页码:1051 / 1055
页数:5
相关论文
共 50 条
[31]   Association between UGT1A1*28*28 genotype and lung cancer in the Japanese population [J].
Nishikawa, Yoshitaka ;
Kanai, Masashi ;
Narahara, Maiko ;
Tamon, Akiko ;
Brown, J. B. ;
Taneishi, Kei ;
Nakatsui, Masahiko ;
Okamoto, Kazuya ;
Uneno, Yu ;
Yamaguchi, Daisuke ;
Tomono, Teruko ;
Mori, Yukiko ;
Matsumoto, Shigemi ;
Okuno, Yasushi ;
Muto, Manabu .
INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2017, 22 (02) :269-273
[32]   UGT1A1*28 is Associated with Decreased Systemic Exposure of Atorvastatin Lactone [J].
Stormo, Camilla ;
Bogsrud, Martin P. ;
Hermann, Monica ;
Asberg, Anders ;
Piehler, Armin P. ;
Retterstol, Kjetil ;
Kringen, Marianne K. .
MOLECULAR DIAGNOSIS & THERAPY, 2013, 17 (04) :233-237
[33]   Screening of patients with Gilbert's Syndrome from South India identifies UGT1A1*28 as the most predominant mutation in UGT1A1 gene [J].
Iyer, Dhanya Ramakrishna ;
Parani, Madasamy .
RESEARCH JOURNAL OF BIOTECHNOLOGY, 2018, 13 (04) :37-40
[34]   Association between uridin diphosphate glucuronosylotransferase 1A1 (UGT1A1) gene polymorphism and neonatal hyperbilirubinemia [J].
Mazur-Kominek, Katarzyna ;
Romanowski, Tomasz ;
Bielawski, Krzysztof ;
Kielbratowska, Bogumila ;
Preis, Krzysztof ;
Domzalska-Popadiuk, Iwona ;
Slominska-Fraczek, Magdalena ;
Sznurkowska, Katarzyna ;
Renke, Joanna ;
Plata-Nazar, Katarzyna ;
Sledzinska, Karolina ;
Sikorska-Wisniewska, Grazyna ;
Gora-Gebka, Magdalena ;
Liberek, Anna .
ACTA BIOCHIMICA POLONICA, 2017, 64 (02) :351-356
[35]   Raloxifene glucuronidation in liver and intestinal microsomes of humans and monkeys: contribution of UGT1A1, UGT1A8 and UGT1A9 [J].
Kishi, Naoki ;
Takasuka, Akane ;
Kokawa, Yuki ;
Isobe, Takashi ;
Taguchi, Maho ;
Shigeyama, Masato ;
Murata, Mikio ;
Suno, Manabu ;
Hanioka, Nobumitsu .
XENOBIOTICA, 2016, 46 (04) :289-295
[36]   Evidence for phosphorylation requirement for human bilirubin UDP-glucuronosyltransferase (UGT1A1) activity [J].
Basu, NK ;
Kole, L ;
Owens, IS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (01) :98-104
[37]   Raloxifene Glucuronidation in Human Intestine, Kidney, and Liver Microsomes and in Human Liver Microsomes Genotyped for the UGT1A1☆28 Polymorphism [J].
Lusin, Tina Trdan ;
Trontelj, Jurij ;
Mrhar, Ales .
DRUG METABOLISM AND DISPOSITION, 2011, 39 (12) :2347-2354
[38]   A Humanized UGT1 Mouse Model Expressing the UGT1A1*28 Allele for Assessing Drug Clearance by UGT1A1-Dependent Glucuronidation [J].
Cai, Hongliang ;
Nguyen, Nghia ;
Peterkin, Vincent ;
Yang, Young-Sun ;
Hotz, Kathy ;
La Placa, Deirdre Beaton ;
Chen, Shujuan ;
Tukey, Robert H. ;
Stevens, Jeffrey C. .
DRUG METABOLISM AND DISPOSITION, 2010, 38 (05) :879-886
[39]   Prevalence of UGT1A1 Gene Polymorphism in Patients with Hemolytic Anemia in Southern Brazil [J].
de Azevedo, Laura Alencastro ;
Santin, Ana Paula ;
Wagner, Sandrine Comparsi ;
Zaleski, Carina da Fontoura ;
Bock, Hugo ;
Saraiva-Pereira, Maria Luiza ;
de Castro, Simone Martins .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2011, 15 (1-2) :107-110
[40]   Limited influence of UGT1A1*28 and no effect of UGT2B7*2 polymorphisms on UGT1A1 or UGT2B7 activities and protein expression in human liver microsomes [J].
Peterkin, Vincent C. ;
Bauman, Jonathan N. ;
Goosen, Theunis C. ;
Menning, Lee ;
Man, Michael Z. ;
Paulauskis, Joseph D. ;
Williams, J. Andrew ;
Myrand, Scott P. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2007, 64 (04) :458-468