2005
DOI: 10.1016/j.cancergencyto.2004.12.005
|View full text |Cite
|
Sign up to set email alerts
|

Genetic polymorphism in the sulfotransferase SULT1A1 gene in cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
16
1

Year Published

2007
2007
2014
2014

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 17 publications
(18 citation statements)
references
References 26 publications
1
16
1
Order By: Relevance
“…Sulfonation is thought to be a detoxification pathway for various xenobiotics, and it is also involved in the bioactivation of several carcinogens by O-esterification to form DNA-damaging toxic metabolites [8,11]. The G to A polymorphism at position 638 of SULT1A1 may result in reduced enzyme activity and reduced thermostability.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Sulfonation is thought to be a detoxification pathway for various xenobiotics, and it is also involved in the bioactivation of several carcinogens by O-esterification to form DNA-damaging toxic metabolites [8,11]. The G to A polymorphism at position 638 of SULT1A1 may result in reduced enzyme activity and reduced thermostability.…”
Section: Discussionmentioning
confidence: 99%
“…In particular, SULT1A1 appears to be a key phenol SULT because of its abundance and distribution in a wide range of tissues [10]. The common polymorphism of SULT1A1 involves a single nucleotide G to A transition at nucleotide 638 (codon 213) in exon 7, which results in an arginine (Arg) to histidine (His) amino acid substitution and this polymorphism may lead to a lower enzyme activity and thermostability [11]. Epidemiological studies have shown inconsistent results for the association between the SULT1A1 G638A polymorphism and several malignancies including bladder cancer, lung cancer and breast cancer [12][13][14][15].…”
Section: Introductionmentioning
confidence: 99%
“…A functional polymorphism in exon 7 of the SULT1A1 gene, with a G→A substitution, results in a change in the amino acid sequence from arginine to histidine, leading to a decrease in enzymatic activity and variable rates of activation or detoxification of procarcinogens (10,11). Carcinogenic aromatic amines, such as 4-aminobiphenyl, which is contained in tobacco smoke, are one of the causal factors of UC.…”
Section: Introductionmentioning
confidence: 99%
“…Cytosolic sulfotransferases (SULT) catalyze the conjugation of sulfo group to these substrates (6), the two major gene families being the phenol (SULT1A1) and hydroxysteroid (SULT2A) sulfotransferases. The SULT1A1 gene is located on chromosome 16p12.1-p11.2 and is expressed in several tissues including liver, lung, and kidney (6). A polymorphism (G!A) in exon 7 of the gene results in substitution of an arginine residue by histidine, decreased enzymatic activity, and changes in mutagen and procarcinogen detoxification and bioactivation rates (6)(7)(8).…”
Section: Introductionmentioning
confidence: 99%
“…The SULT1A1 gene is located on chromosome 16p12.1-p11.2 and is expressed in several tissues including liver, lung, and kidney (6). A polymorphism (G!A) in exon 7 of the gene results in substitution of an arginine residue by histidine, decreased enzymatic activity, and changes in mutagen and procarcinogen detoxification and bioactivation rates (6)(7)(8). The variant allele SULT1A1*2 with reduced sulfotransferase activity might enhance the risk of cancer (6).…”
Section: Introductionmentioning
confidence: 99%