EFFECTS OF LOW-DOSES OF N-NITROSOMORPHOLINE ON THE DEVELOPMENT OF EARLY STAGES OF HEPATOCARCINOGENESIS

被引:35
作者
ENZMANN, H
ZERBAN, H
KOPPSCHNEIDER, A
LOSER, E
BANNASCH, P
机构
[1] GERMAN CANC RES CTR,DEPT BIOSTAT,D-69120 HEIDELBERG,GERMANY
[2] GERMAN CANC RES CTR,DIV CELL PATHOL,D-69120 HEIDELBERG,GERMANY
关键词
D O I
10.1093/carcin/16.7.1513
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Male Sprague-Dawley rats received the hepatocarcinogen N-nitrosomorpholine (NNM) in the drinking water at low dose levels ranging from 6 mg/l to 60 mg/l for 6 and 12 weeks, respectively. Foci of altered hepatocytes (FAH) were demonstrated histochemically using changes in the activities of glucose-6-phosphate dehydrogenase and glycogen phosphorylase, and in the glycogen content as markers. Proliferating cells were detected by the immunohistochemical reaction for proliferating cell nuclear antigen (PCNA), The number and size of foci of altered hepatocytes increased in a time and dose-related manner, The dose-effect curves were non-linear with a slight positive slope at the low doses and a markedly increased slope at higher doses, The number of PCNA positive hepatocytes showed a dose-dependent increase, In addition to the granular distribution of PCNA in the nuclei, hepatocyte nuclei with homogeneously distributed PCNA occurred in animals exposed to 60 mg/l NNM, It is proposed that these cells are related to the occurrence of hepatocytes with higher ploidy induced by NNM and may be regarded as cells in the G2 phase of the cell cycle, The non-linear shape of the dose-response-curve of the FAH suggests that some mechanisms contribute to carcinogenesis over the whole dose range, whereas other mechanisms enhance carcinogenesis only at higher doses. The relevance of the non-linear dose-effect curve for the risk assessment of carcinogens is discussed.
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页码:1513 / 1518
页数:6
相关论文
共 51 条
[1]   CHEMICAL CANCEROGENESIS - DEFINITIONS OF FREQUENTLY USED TERMS [J].
APPEL, KE ;
FURSTENBERGER, G ;
HAPKE, HJ ;
HECKER, E ;
HILDEBRANDT, AG ;
KORANSKY, W ;
MARKS, F ;
NEUMANN, HG ;
OHNESORGE, FK ;
SCHULTEHERMANN, R .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1990, 116 (03) :232-236
[2]   TIGROID CELL FOCI AND NEOPLASTIC NODULES IN THE LIVER OF RATS TREATED WITH A SINGLE DOSE OF AFLATOXIN-B1 [J].
BANNASCH, P ;
BENNER, U ;
ENZMANN, H ;
HACKER, HJ .
CARCINOGENESIS, 1985, 6 (11) :1641-1648
[3]   PRENEOPLASTIC LESIONS AS END-POINTS IN CARCINOGENICITY TESTING .1. HEPATIC PRENEOPLASIA [J].
BANNASCH, P .
CARCINOGENESIS, 1986, 7 (05) :689-695
[4]  
Bannasch P., 1968, RECENT RES CANCER, V19, P1
[5]   A NEW, QUANTITATIVE, APPROACH TO THE STUDY OF THE STAGES OF CHEMICAL CARCINOGENESIS IN THE MOUSES SKIN [J].
BERENBLUM, I ;
SHUBIK, P .
BRITISH JOURNAL OF CANCER, 1947, 1 (04) :383-391
[6]   COMBINATION EXPERIMENTS WITH VERY LOW-DOSES OF 3 GENOTOXIC N-NITROSAMINES WITH SIMILAR ORGANOTROPIC CARCINOGENICITY IN RATS [J].
BERGER, MR ;
SCHMAHL, D ;
ZERBAN, H .
CARCINOGENESIS, 1987, 8 (11) :1635-1643
[7]   PERSISTENT PROLIFERATION OF NORMAL HEPATOCYTES AND PROMOTION OF PRENEOPLASTIC DEVELOPMENT BY N-NITROSODIBENZYLAMINE IN RATS [J].
BLASZYK, H ;
HARTMANN, A ;
DANZ, M .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1993, 120 (1-2) :71-75
[8]   INITIATION OF CHEMICAL CARCINOGENESIS REQUIRES CELL-PROLIFERATION [J].
CAYAMA, E ;
TSUDA, H ;
SARMA, DSR ;
FARBER, E .
NATURE, 1978, 275 (5675) :60-62
[9]   INCREASED NUCLEAR CYCLIN/PCNA ANTIGEN STAINING OF NON S-PHASE TRANSFORMED HUMAN AMNION CELLS ENGAGED IN NUCLEOTIDE EXCISION DNA-REPAIR [J].
CELIS, JE ;
MADSEN, P .
FEBS LETTERS, 1986, 209 (02) :277-283
[10]  
CRUMP KS, 1976, CANCER RES, V36, P2973