INVITRO TRANSFORMATION OF BALB/C 3T3 CELLS BY 1,1,2,2-TETRACHLOROETHANE

被引:16
作者
COLACCI, A
PEROCCO, P
VACCARI, M
MAZZULLO, M
ALBINI, A
PARODI, S
TANINGHER, M
GRILLI, S
机构
[1] UNIV BOLOGNA,CTR INTERUNIV RIC CANC,IST CANCEROL,VIALE FILOPANTI 22,I-40126 BOLOGNA,ITALY
[2] UNIV BOLOGNA,IST CANCEROL,IST NAZL RIC CANC,IST SCI TUMORI GENOVA,I-40126 BOLOGNA,ITALY
[3] IST NAZL RIC CANC,IST SCI TUMORI GENOVA,SERV CANC GENESI CHIM,I-16132 GENOA,ITALY
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1990年 / 81卷 / 08期
关键词
1,1,2,2‐Tetrachloroethane; BALB/c; 3T3; Transformation;
D O I
10.1111/j.1349-7006.1990.tb02646.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
1,1,2,2‐Tetrachloroethane (1,1,2,2‐TTCE) was shown to be capable of inducing in vitro transformation of BALB/c 3T3 cells (clone A‐31) either in the presence or in the absence of S9 activating system using an amplification‐transformation (level‐II) assay by reseeding confluent cells from each treatment and allowing additional rounds of cell replication. In the absence of metabolic activation, the highest assayed dose (1000 μg/ml), exerting the highest toxicity, was the only transforming dose. Lower doses of 1,1,2,2‐TTCE were capable of transforming BALB/c cells in the presence of S9 activating system, the dose of 500 μg/ml exerting the highest transforming activity. The number and size of transformed foci recognized in the level‐II plates were a function of the number of cells reseeded in the amplification assay. Foci obtained in the presence of S9 activating systems were larger in size, more deeply basophilic, and exhibited denser multilayering of constituent cells than foci recognized in the absence of exogenous metabolic activation. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:786 / 792
页数:7
相关论文
共 19 条
[1]   INVIVO AND INVITRO BINDING OF 1,2-DIBROMOETHANE AND 1,2-DICHLOROETHANE TO MACROMOLECULES IN RAT AND MOUSE ORGANS [J].
ARFELLINI, G ;
BARTOLI, S ;
COLACCI, A ;
MAZZULLO, M ;
GALLI, MC ;
PRODI, G ;
GRILLI, S .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1984, 108 (02) :204-213
[2]   INVITRO MICROSOME-MEDIATED AND CYTOSOL-MEDIATED BINDING OF 1,2-DICHLOROETHANE AND 1,2-DIBROMOETHANE WITH DNA [J].
COLACCI, A ;
MAZZULLO, M ;
ARFELLINI, G ;
PRODI, G ;
GRILLI, S .
CELL BIOLOGY AND TOXICOLOGY, 1985, 1 (02) :45-55
[3]   THE COVALENT BINDING OF 1,1,2,2-TETRACHLOROETHANE TO MACROMOLECULES OF RAT AND MOUSE ORGANS [J].
COLACCI, A ;
GRILLI, S ;
LATTANZI, G ;
PRODI, G ;
TURINA, MP ;
FORTI, GC ;
MAZZULLO, M .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1987, 7 (05) :465-474
[4]   CELL-TRANSFORMATION BY CHEMICAL-AGENTS - A REVIEW AND ANALYSIS OF THE LITERATURE - A REPORT OF THE UNITED-STATES-ENVIRONMENTAL-PROTECTION-AGENCY GENE-TOX PROGRAM [J].
HEIDELBERGER, C ;
FREEMAN, AE ;
PIENTA, RJ ;
SIVAK, A ;
BERTRAM, JS ;
CASTO, BC ;
DUNKEL, VC ;
FRANCIS, MW ;
KAKUNAGA, T ;
LITTLE, JB ;
SCHECHTMAN, LM .
MUTATION RESEARCH, 1983, 114 (03) :283-385
[5]  
INSKEEP PB, 1986, CANCER RES, V46, P2839
[6]   INVIVO COVALENT BINDING OF ORGANIC-CHEMICALS TO DNA AS A QUANTITATIVE INDICATOR IN THE PROCESS OF CHEMICAL CARCINOGENESIS [J].
LUTZ, WK .
MUTATION RESEARCH, 1979, 65 (04) :289-356
[7]   CHEMICAL MECHANISMS OF HALOCARBON METABOLISM [J].
MACDONALD, TL .
CRC CRITICAL REVIEWS IN TOXICOLOGY, 1983, 11 (02) :85-120
[8]   RAT-LIVER FOCI AND INVITRO ASSAYS TO DETECT INITIATING AND PROMOTING EFFECTS OF CHLORINATED ETHANES AND ETHYLENES [J].
MILMAN, HA ;
STORY, DL ;
RICCIO, ES ;
SIVAK, A ;
TU, AS ;
WILLIAMS, GM ;
TONG, C ;
TYSON, CA .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 534 :521-530
[9]  
PARODI S, 1984, SISTER CHROMATID EXC, P409
[10]  
PRODI G, 1988, CHEM CARCINOGENESIS, P93