STUDIES IN GASTRIC CARCINOGENESIS .4. O-6-METHYLGUANINE AND ITS REPAIR IN NORMAL AND ATROPHIC BIOPSY SPECIMENS OF HUMAN GASTRIC-MUCOSA - CORRELATION OF O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE ACTIVITIES IN GASTRIC-MUCOSA AND CIRCULATING LYMPHOCYTES

被引:35
作者
KYRTOPOULOS, SA
AMPATZI, P
DAVARIS, P
HARITOPOULOS, N
GOLEMATIS, B
机构
[1] UNIV ATHENS,SCH MED,ANAT & PHYSIOL LAB,ATHENS,GREECE
[2] UNIV ATHENS,PREPEDEUT SURG CLIN 1,ATHENS,GREECE
关键词
D O I
10.1093/carcin/11.3.431
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
DNA extracted from biopsies of normal or atrophic gastric mucosa obtained from 20 individuals was analysed for the presence of the precarcinogenic alkylation lesion O6-methylguanine by a recently developed, highly sensitive assay based on repair by the Escherichia coli O6-alkylguanine-DNA alkyltransferase (AGT) enzyme in competition with a radiolabelled oligonucleotide containing O6-methylguanine (O6-meG). With a limit of detection of 0.5 fmol O6-meG in 10 μg DNA, only one DNA sample (derived from a region of the stomach with advanced chronic atrophic gastritis) was found marginally positive, containing 0.52 fmol/10 μg DNA (8.3 × 10-8 mol O6-meG/mol guanine). Measurements of AGT in 49 biopsies of normal, atrophic, hyperplastic or dysplastic mucosa obtained from the gastric antrum or corpus of 18 individuals did not reveal any significant effects of mucosal Histology on AGT. The average AGT value found was 6.9 ± 3.5 (SD) fmol/μg DNA, which is lower than the values reported for a number of other human tissues (liver, small intestine and lung). Measurement of AGT levels in gastric mucosa and circulating lymphocytes of the same individuals revealed a psitive correlation (P < 0.005), suggesting that lymphocytes may serve as a useful surrogate marker for AGT activity in gastric mucosa in studies of the epidemiology of this important repair enzyme. © 1990 Oxford University Press.
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页码:431 / 436
页数:6
相关论文
共 37 条
[1]  
BEDELL MA, 1982, CANCER RES, V42, P3079
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]  
BURTON K, 1956, BIOCHEM J, V62, P123
[4]  
CHARNLEY G, 1982, BANBURY REPORT, V12, P503
[5]  
CORREA P, 1983, CANCER SURV, V2, P437
[6]  
CORREA P, 1975, LANCET, V2, P58
[7]  
CRESPI M, 1987, RELEVANCE N NITROSO, P511
[8]   USE OF A DODECADEOXYNUCLEOTIDE TO STUDY REPAIR OF THE O-4-METHYLTHYMINE LESION [J].
DOLAN, ME ;
OPLINGER, M ;
PEGG, AE .
MUTATION RESEARCH, 1988, 193 (02) :131-137
[9]  
FOILES PG, 1988, CANCER RES, V48, P4184
[10]  
GERSON SL, 1988, CANCER RES, V48, P5368