1999
DOI: 10.1007/s101200050040
|View full text |Cite
|
Sign up to set email alerts
|

Genotypes of glutathione S-transferase M1 and N-acetyltransferase 2 in Japanese patients with gastric cancer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
8
0

Year Published

2004
2004
2011
2011

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 21 publications
(9 citation statements)
references
References 34 publications
1
8
0
Order By: Relevance
“…21,23 The PCR reaction mixture was electrophoresed on a 2% agarose gel to verify the successful multiplication of the -globin gene and to identify whether or not a PCR product derived from the GSTM1 gene was present. 21,23 A set of oligonucleotide primers was used to amplify the 559-bp NAT2 genomic sequence. The 559-bp PCR product was digested by Bam HI and Asp 718.…”
Section: Genotypingmentioning
confidence: 99%
See 2 more Smart Citations
“…21,23 The PCR reaction mixture was electrophoresed on a 2% agarose gel to verify the successful multiplication of the -globin gene and to identify whether or not a PCR product derived from the GSTM1 gene was present. 21,23 A set of oligonucleotide primers was used to amplify the 559-bp NAT2 genomic sequence. The 559-bp PCR product was digested by Bam HI and Asp 718.…”
Section: Genotypingmentioning
confidence: 99%
“…The genotypes of the CYP2E1 gene were identified by restriction fragment length polymorphism: 20 the PCR-amplified DNA fragments, including the polymorphic site, were digested with Rsa I, and subjected to electrophoresis on 2.0% agarose gel. Identification of the GSTM1 and NAT2 genotypes was performed according to the methods of Kempkes et al, 21 Abe et al, 22 and Oda et al 23 Two sets of oligonucleotide primers were used to amplify simultaneously the polymorphic GSTM1 and a segment of -globin. 21,23 The PCR reaction mixture was electrophoresed on a 2% agarose gel to verify the successful multiplication of the -globin gene and to identify whether or not a PCR product derived from the GSTM1 gene was present.…”
Section: Genotypingmentioning
confidence: 99%
See 1 more Smart Citation
“…The NAT2 rapid acetylator phenotype is thought to be indicative of higher risk, because N-acetylation is negligible and O-acetylation is an activation step for PhIP and MeIQx association with several cancers [15,16]. However, no consistent association between the NAT2 phenotype or genotype and stomach cancer risk has been identifi ed [17][18][19][20][21][22][23]. No investigation of the combined effect of well-done meat and HCA intake with the NAT2 phenotype or genotype has appeared.…”
Section: Discussionmentioning
confidence: 99%
“…Japanese researchers suggested that a combination of GSTM1 and NAT2 decreases the risk of gastric cancer in Japanese patients [69] . A population-based case-control study in China suggested that the GSTP1 genotype seems not to be associated with the risk of gastric cancer and chronic gastritis in a high-risk Chinese population [70] .…”
Section: Genetic Polymorphisms Of Some Metabolizing Enzymesmentioning
confidence: 99%