Sulfotransferase genetic variation: from cancer risk to treatment response

被引:32
作者
Daniels, Jaclyn [1 ]
Kadlubar, Susan [1 ]
机构
[1] Univ Arkansas Med Sci, Coll Med, Dept Med Genet, Little Rock, AR 72205 USA
关键词
Breast cancer; cancer survival; environmental exposures; gene gene interactions; tamoxifen; SULT1A1 ARG(213)HIS POLYMORPHISM; CARCINOGEN-METABOLIZING ENZYMES; COMMON GERMLINE POLYMORPHISMS; ISOFORM; 1A1; SULT1A1; PHENOL SULFOTRANSFERASE; BLADDER-CANCER; CYTOSOLIC SULFOTRANSFERASES; MOLECULAR-CLONING; PROSTATE-CANCER; 5'-FLANKING REGION;
D O I
10.3109/03602532.2013.835621
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cytosolic sulfotransferases (SULTs) are phase II detoxification enzymes that are involved in the biotransformation of a wide variety of structurally diverse endo- and xenobiotics. Single-nucleotide polymorphisms (SNPs) in SULTs can alter the phenotype of the translated proteins. SNPs in some SULTs are fairly uncommon in the population, but some, most notably for SULT isoform 1A1, are commonly found and have been associated with cancer risk for a variety of tumor sites and also with response to therapeutic agents. SNPs in many SULTs vary by ethnicity, another factor that could influence SULT-associated disease risk and pharmacogenetics. This review surveys the current knowledge of SULT genetic variability in relation to cancer risk and response to therapy, focusing primarily on SULT1A1.
引用
收藏
页码:415 / 422
页数:8
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