Evaluation of the rodent micronucleus assay in the screening of IARC carcinogens (Groups 1, 2A and 2B) - The summary report of the 6th collaborative study by CSGMT/JEMS center dot MMS

被引:196
作者
Morita, T
Asano, N
Awogi, T
Sasaki, YF
Sato, S
Shimada, H
Sutou, S
Suzuki, T
Wakata, A
Sofuni, T
Hayashi, M
机构
[1] NITTO DENKO CORP, BIOCHEM RES LAB, IBARAKI, OSAKA 567, JAPAN
[2] NIPPON GLAXO LTD, TSUKUBA RES LABS, TSUKUBA, IBARAKI 30042, JAPAN
[3] OTSUKA PHARMACEUT CO LTD, DRUG SAFETY RES CTR, TOKUSHIMA 77101, JAPAN
[4] HACHINOHE INST TECHNOL, FAC CHEM & BIOL ENGN, HACHINOHE, AOMORI 03911, JAPAN
[5] JAPAN TOBACCO INC, TOXICOL RES LABS, HADANO, KANAGAWA 257, JAPAN
[6] DAIICHI PHARMACEUT CO LTD, DEV RES LABS, EDOGAWA KU, TOKYO 134, JAPAN
[7] ITOHAM FOODS INC, GEN RES INST, IBARAKI, OSAKA 30201, JAPAN
[8] NATL INST HLTH SCI, DIV GENET & MUTAGENESIS, SETAGAYA KU, TOKYO 158, JAPAN
[9] YAMANOUCHI PHARMACEUT CO LTD, PROD DEV LABS, ITABASHI KU, TOKYO 174, JAPAN
关键词
micronucleus test; IARC monograph; human carcinogen; CSGMT;
D O I
10.1016/S1383-5718(96)00070-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To assess the correlation between micronucleus induction and human carcinogenicity, the rodent micronucleus assay was performed on known and potential human carcinogens in the 6th MMS/CSGMT collaborative study, Approximately 100 commercially available chemicals and chemical groups on which there was little or no micronucleus assay data were selected from IARC (International Agency for Research on Cancer) Groups 1 (human carcinogen), 2A (probable human carcinogen) and 2B (possible human carcinogen), As minimum requirements for the collaborative study, 5 male mice were treated by intraperitoneal injection or oral gavage once or twice with each chemical at three dose levels, and bone marrow and/or peripheral blood was analyzed. Five positives and 2 inconclusives out of 13 Group 1 chemicals, 7 positives and 5 inconclusives of 23 Group 2A chemicals, and 26 positives and 6 inconclusives of 67 Group 2B chemicals were found. Such low positive rates were not surprising because of a test chemical selection bias, and we excluded well-known micronucleus inducers, The overall evaluation of the rodent micronucleus assay was based on the present data combined with published data on the IARC carcinogens. After merging, the positive rates for Groups 1, 2A and 2B were 68.6, 54.5 and 45.6%, respectively. Structure-activity relationship analysis suggested that the micronucleus assay is more sensitive to the genetic toxicity of some classes of chemicals. Those to which it is sensitive consist of (1) aziridines and bis(2-chloroethyl) compounds; (2) alkyl sulfonate and sulfates; (3) acyl-type N-nitroso compounds; (4) hydrazines; (5) aminobiphenyl and benzidine derivatives; and (6) azo compounds. Those to which it is less sensitive consist of (1) dialkyl type N-nitroso compounds; (2) silica and metals and their compounds; (3) aromatic amines without other functional groups; (4) halogenated compounds; and (5) steroids and other hormones. After incorporation of structure-activity relationship information, the positive rates of the rodent micronucleus assay became 90.5, 65.2 and 60.0% for IARC Groups 1, 2A and 2B, respectively. Noteworthy was the tendency of the test to be more sensitive to those carcinogens with stronger evidence human carcinogenicity.
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页码:3 / 122
页数:120
相关论文
共 232 条
[71]   INVITRO MUTAGENICITY AND CELL-TRANSFORMATION SCREENING OF PHENYLGLYCIDYL ETHER [J].
GREENE, EJ ;
FRIEDMAN, MA ;
SHERROD, JA ;
SALERNO, AJ .
MUTATION RESEARCH, 1979, 67 (01) :9-19
[72]   GENOTOXICITY OF TAUROMUSTINE, A NEW WATER-SOLUBLE TAURINE-BASED NITROSOUREA .1. MUTAGENIC AND CLASTOGENIC ACTIVITY OF TAUROMUSTINE INVITRO [J].
HARTLEYASP, B .
MUTAGENESIS, 1992, 7 (06) :427-431
[73]   SALMONELLA MUTAGENICITY TEST-RESULTS FOR 250 CHEMICALS [J].
HAWORTH, S ;
LAWLOR, T ;
MORTELMANS, K ;
SPECK, W ;
ZEIGER, E .
ENVIRONMENTAL MUTAGENESIS, 1983, 5 :3-&
[74]   IN-VIVO RODENT ERYTHROCYTE MICRONUCLEUS ASSAY [J].
HAYASHI, M ;
TICE, RR ;
MACGREGOR, JT ;
ANDERSON, D ;
BLAKEY, DH ;
KIRSHVOLDERS, M ;
OLESON, FB ;
PACCHIEROTTI, F ;
ROMAGNA, F ;
SHIMADA, H ;
SUTOU, S ;
VANNIER, B .
MUTATION RESEARCH, 1994, 312 (03) :293-304
[75]   STATISTICAL-ANALYSIS OF DATA IN MUTAGENICITY ASSAYS - RODENT MICRONUCLEUS ASSAY [J].
HAYASHI, M ;
HASHIMOTO, S ;
SAKAMOTO, Y ;
HAMADA, C ;
SOFUNI, T ;
YOSHIMURA, I .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :49-52
[76]   DIFFERENCE BETWEEN INTRAPERITONEAL AND ORAL GAVAGE APPLICATION IN THE MICRONUCLEUS TEST - THE 3RD COLLABORATIVE STUDY BY CSGMT JEMS MMS [J].
HAYASHI, M ;
SUTOU, S ;
SHIMADA, H ;
SATO, S ;
SASAKI, YF ;
WAKATA, A .
MUTATION RESEARCH, 1989, 223 (04) :329-344
[77]   A PROCEDURE FOR DATA-ANALYSIS OF THE RODENT MICRONUCLEUS TEST INVOLVING A HISTORICAL CONTROL [J].
HAYASHI, M ;
YOSHIMURA, I ;
SOFUNI, T ;
ISHIDATE, M .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1989, 13 (04) :347-356
[78]   HIGH-SENSITIVITY IN MICRONUCLEUS INDUCTION OF A MOUSE STRAIN (MS) [J].
HAYASHI, M ;
SOFUNI, T ;
ISHIDATE, M .
MUTATION RESEARCH, 1982, 105 (04) :253-256
[79]   2-(2-FURYL)-3-(5-NITRO-2-FURYL)ACRYLAMIDE (AF-2) IS A WEAK IN-VIVO CLASTOGEN AS REVEALED BY THE MICRONUCLEUS ASSAY [J].
HIGASHIKUNI, N ;
HARA, M ;
NAKAGAWA, S ;
SUTOU, S .
MUTATION RESEARCH, 1994, 320 (1-2) :149-156
[80]   AN OPTIMAL, GENERALIZED SAMPLING TIME OF 30+/-6 H AFTER DOUBLE DOSING IN THE MOUSE PERIPHERAL-BLOOD MICRONUCLEUS TEST [J].
HIGASHIKUNI, N ;
SUTOU, S .
MUTAGENESIS, 1995, 10 (04) :313-319