Genetic polymorphism of cytochrome P450 1A1 (CYP1A1) and glutathione transferases (M1, T1 and P1) among Africans

被引:38
作者
Dandara, C
Sayi, J
Masimirembwa, CM
Magimba, A
Kaaya, S
De Sommers, K
Snyman, JR
Hasler, JA
机构
[1] Univ Zimbabwe, Dept Biochem, Harare, Zimbabwe
[2] Muhimbili Coll Hlth Sci, Dept Pharmacol, Dar Es Salaam, Tanzania
[3] Univ Pretoria, Dept Pharmacol, ZA-0001 Pretoria, South Africa
关键词
gene polymorphism; Africans; cytochrome P450; glutathione transferase;
D O I
10.1515/CCLM.2002.167
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The coordinate expression and regulation of the drug metabolising enzymes, cytochrome P4501A1 (CYP1A1) and glutathione transferases (GSTM1, GSTT1 and GSTP1), and their metabolic balance in the cells of target organs may determine whether exposure to carcinogens results in cancer. Besides showing variability in activity due to induction and inhibition, these enzymes also exhibit genetic polymorphism that alter enzyme levels and activity. We determined frequencies of common allelic variants of CYP1A1 and glutathione (M1, T1 and P1) among Tanzanians, South African Venda and Zimbabweans using PCR/restriction fragment length polymorphism techniques. The CYP1A1 Val462 mutant variant was found at a frequency of 1.3% among 114 subjects. The GSTM1*0 genotype was found at a frequency of 29% and 33% among Tanzanian psychiatric patients and healthy volunteers, respectively. Similarly, the GSTT1*0 polymorphism was present with a frequency of 25% in both the psychiatric patients and healthy controls. The frequency of GSTP1 Val105 variant was 16%, 12% and 21% among Tanzanians, South African Venda and Zimbabweans, respectively. We conclude here that CYP1A1 Val462 polymorphism is very rare among Africans. This is the first report of the GSTP1 Val105 variant frequency in African populations. We show here that there are no differences in frequencies of the variant alleles for CYP1A1, GSTM1, GSTT1 and GSTP1 in the three African populations.
引用
收藏
页码:952 / 957
页数:6
相关论文
共 44 条
[1]   GENETIC SUSCEPTIBILITY TO LUNG-CANCER WITH SPECIAL EMPHASIS ON CYP1A1 AND GSTM1 - A STUDY ON HOST FACTORS IN RELATION TO AGE AT ONSET, GENDER AND HISTOLOGICAL CANCER TYPES [J].
ALEXANDRIE, AK ;
SUNDBERG, MI ;
SEIDEGARD, J ;
TORNLING, G ;
RANNUG, A .
CARCINOGENESIS, 1994, 15 (09) :1785-1790
[2]  
AliOsman F, 1997, J BIOL CHEM, V272, P10004
[3]   ISOLATION OF A CDNA CLONE AND LOCALIZATION OF THE HUMAN GLUTATHIONE S-TRANSFERASE 3-GENES TO CHROMOSOME BANDS 11Q13 AND 12Q13-14 [J].
BOARD, PG ;
WEBB, GC ;
COGGAN, M .
ANNALS OF HUMAN GENETICS, 1989, 53 :205-213
[4]   CORRELATION BETWEEN TRANS-STILBENE OXIDE-GLUTATHIONE CONJUGATION ACTIVITY AND THE DELETION MUTATION IN THE GLUTATHIONE-S-TRANSFERASE CLASS MU GENE DETECTED BY POLYMERASE CHAIN-REACTION [J].
BROCKMOLLER, J ;
GROSS, D ;
KERB, R ;
DRAKOULIS, N ;
ROOTS, I .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (03) :647-650
[5]   RELEVANCE OF METABOLIC POLYMORPHISMS TO HUMAN CARCINOGENESIS - EVALUATION OF EPIDEMIOLOGIC EVIDENCE [J].
CAPORASO, N ;
LANDI, MT ;
VINEIS, P .
PHARMACOGENETICS, 1991, 1 (01) :4-19
[6]   RECONSTRUCTION OF HUMAN-EVOLUTION - BRINGING TOGETHER GENETIC, ARCHAEOLOGICAL, AND LINGUISTIC DATA [J].
CAVALLISFORZA, LL ;
PIAZZA, A ;
MENOZZI, P ;
MOUNTAIN, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :6002-6006
[7]   Simultaneous characterization of glutathione S-transfersase M1 and T1 polymorphisms by polymerase chain reaction in American whites and blacks [J].
Chen, CL ;
Liu, Q ;
Relling, MV .
PHARMACOGENETICS, 1996, 6 (02) :187-191
[8]   GLUTATHIONE-S-TRANSFERASE M1 AND T1 POLYMORPHISMS - SUSCEPTIBILITY TO COLON-CANCER AND AGE-OF-ONSET [J].
CHENEVIXTRENCH, G ;
YOUNG, J ;
COGGAN, M ;
BOARD, P .
CARCINOGENESIS, 1995, 16 (07) :1655-1657
[9]  
DALY AK, 1995, J MOL MED-JMM, V73, P539
[10]  
DALY AK, 1994, ENV HLTH PERSPECT, V102, P5