The investigation of GSTT1, GSTM1 and SOD polymorphism in bladder cancer patients

被引:26
作者
Cengiz, Muejgan
Ozaydin, Ahmet
Ozkilic, Anil Cagla
Dedekarginoglu, Galip
机构
[1] IU Cerhpasa Tip Fak, Temel Bilimler Binasi, TR-34093 Istanbul, Turkey
[2] Istanbul Univ, Cerrahpasa Med Fac, Dept Med Biol, Istanbul, Turkey
[3] SSK Okemeydani Hosp, Dept Urol, Istanbul, Turkey
关键词
bladder cancer; GSTT1; GSTM1; SOD polymorphism;
D O I
10.1007/s11255-007-9179-9
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Glutathione S transferases (GSTT1, GSTM1, GSTP1) are enzymes that activate the detoxification of endogenous and exogenous agents. The genetic polymorphism in these genes may change the response of individuals to environmental toxicants. The genetic polymorphisms of GSTT1, GSTM1, GSTP1 have been studied extensively in the determination of individual cancer risks. Some studies showed a strong relationship between polymorphism of GSTs and superoxidedismutase enzymes. Using the polymerase chain reaction (PCR) the prevalence of genetic polymorphisms of GSTT1, GSTM1 and MnSOD (Manganese Superoxide Dismurase) was investigated in 104 cases and controls to seek any association with the risk of bladder cancer. The frequency of GSTT1 +/+ polymorphism was 65% (33/51) in the cases and 79% (42/53) in the controls. The frequency of the GSTM1 +/+ polymorphism was 33% (17/51) in the cases and 58% (31/53) in the controls. The frequency of the GSTM1 null genotype was 42% (22/53) in the controls and 68% (34/51) in the patients. The frequency of the SOD AA genotype was 36% (17/51) in the cases and 33% (19/53) in the controls. There was no association between the GSTT1 and SOD polymorphism and bladder cancer incidence. The incidence of the GSTM1 null genotype was increased in bladder cancer patients compared to controls (OR = 1.755, 95% CI = 1.119-2.751).
引用
收藏
页码:1043 / 1048
页数:6
相关论文
共 30 条
[1]   Glutathione S-transferase M1 gene polymorphism in bladder cancer patients: a marker for invasive bladder cancer? [J].
Aktas, D ;
Ozen, H ;
Atsu, N ;
Tekin, A ;
Sozen, S ;
Tuncbilek, E .
CANCER GENETICS AND CYTOGENETICS, 2001, 125 (01) :1-4
[2]  
[Anonymous], 1999, J KOREAN CANC ASS
[3]   A multiplex polymerase chain reaction protocol for the simultaneous analysis of the glutathione S-transferase GSTM1 and GSTT1 polymorphisms [J].
Arand, M ;
Muhlbauer, R ;
Hengstler, J ;
Jager, E ;
Fuchs, J ;
Winkler, L ;
Oesch, F .
ANALYTICAL BIOCHEMISTRY, 1996, 236 (01) :184-186
[4]   GLUTATHIONE S-TRANSFERASES - BIOMEDICAL APPLICATIONS [J].
BECKETT, GJ ;
HAYES, JD .
ADVANCES IN CLINICAL CHEMISTRY, VOL 30, 1993, 30 :281-380
[5]   THE GLUTATHIONE S-TRANSFERASES - AN UPDATE [J].
BOYER, TD .
HEPATOLOGY, 1989, 9 (03) :486-496
[6]  
Brockmoller J, 1996, CANCER RES, V56, P3915
[7]  
*CANC RES UK, 2006, BLADD CANC STAG
[8]   Increased risk for myelodysplastic syndromes in individuals with glutathione transferase theta 1 (GSTT1) gene defect [J].
Chen, HW ;
Sandler, DP ;
Taylor, JA ;
Shore, DL ;
Liu, E ;
Bloomfield, CD ;
Bell, DA .
LANCET, 1996, 347 (8997) :295-297
[9]   CTLA4 gene polymorphisms are associated with, and linked to, insulin-dependent diabetes mellitus in a Russian population [J].
Chistiakov, Dimitry A. ;
Savost'anov, Kirill V. ;
Nosikov, Valery V. .
BMC GENETICS, 2001, 2 (1)
[10]  
CORRELIA MA, 2001, LANGE MED BOOK, P52