RELATIONSHIP BETWEEN CHEMICALLY-INDUCED HA-RAS MUTATION AND TRANSFORMATION OF BALB/C 3T3 CELLS - EVIDENCE FOR CHEMICAL-SPECIFIC ACTIVATION AND CELL TYPE SPECIFIC RECRUITMENT OF ONCOGENE IN TRANSFORMATION

被引:41
作者
NAKAZAWA, H
AGUELON, AM
YAMASAKI, H
机构
[1] International Agency for Research on Cancer, Lyon
关键词
BALB/c; 3T3; carcinogen‐specific oncogene activation; codon; 61; DMBA; Ha‐ras; initiation; Ki‐ras; mutation; PCR; tissue‐specific oncogene activation;
D O I
10.1002/mc.2940030407
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BALB/c 3T3 cells were exposed to 7, 12‐dimethylbenz[a]anthracene (DMBA) and resultant transformed foci were analyzed for the presence of A182 → T mutation at codon 61 of Ha‐ras (a mutation found in many DMBA‐induced animal tumors). None of the 30 independently cloned transformed cell lines contained such a mutation. In order to see whether DMBA is able to induce this mutation in BALB/c 3T3 cells, we developed a method sensitive enough to detect this specific mutation at the frequency of 10–6. Employing this assay, we found time‐and dose‐dependent induction by DMBA of Ha‐ras A182 → T mutation in BALB/c 3Tc cells; for example, 2 wk after exposure to 100 μg/mL DMBA, 1.4 in 1 × 104 cells contained this specific mutation. On the other hand, other agents that also induce BALB/c 3T3 cell transformation, such as 3‐methylcholanthrene (MCA), 12‐O‐tetradecanoylphorbol‐13‐acetate (TPA), N‐methyl‐N'‐nitro‐N‐nitrosoguanidine (MNNG), or ultraviolet light, did not induce the mutation at detectable frequency (< 10–6). These results suggest that DMBA efficiently induces Ha‐ras mutation in BALB/c 3T3 cells but that this mutation is not recruited in the process of cell transformation. A hypothesis of carcinogen‐specific mutation of Ha‐ras gene and its tissue (cell type)‐specific recruitment in carcinogenesis is proposed. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:202 / 209
页数:8
相关论文
共 28 条
[1]   ONCOGENE ACTIVATION IN CHEMICAL CARCINOGENESIS [J].
BALMAIN, A ;
BROWN, K .
ADVANCES IN CANCER RESEARCH, 1988, 51 :147-182
[2]   RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[3]  
Barrett J.C., 1985, MECHANISMS TOXICITY, P171
[4]   MUTAGENESIS OF THE HA-RAS ONCOGENE IN MOUSE SKIN TUMORS INDUCED BY POLYCYCLIC AROMATIC-HYDROCARBONS [J].
BIZUB, D ;
WOOD, AW ;
SKALKA, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :6048-6052
[5]  
BOS JL, 1989, CANCER RES, V49, P4682
[6]   CHEMICAL CARCINOGENS AND RAS GENE ACTIVATION [J].
BROOKES, P .
MOLECULAR CARCINOGENESIS, 1989, 2 (06) :305-307
[7]   ISOLATION AND CHARACTERIZATION OF THE 5' FLANKING REGION OF THE MOUSE C-HARVEY-RAS GENE [J].
BROWN, K ;
BAILLEUL, B ;
RAMSDEN, M ;
FEE, F ;
KRUMLAUF, R ;
BALMAIN, A .
MOLECULAR CARCINOGENESIS, 1988, 1 (03) :161-170
[8]   CANCER GENES - RARE RECOMBINANTS INSTEAD OF ACTIVATED ONCOGENES (A REVIEW) [J].
DUESBERG, PH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2117-2124
[9]   DETECTION OF NON-GENOTOXIC CARCINOGENS IN THE BALB/C 3T3 CELL-TRANSFORMATION MUTATION ASSAY SYSTEM [J].
FITZGERALD, DJ ;
PICCOLI, C ;
YAMASAKI, H .
MUTAGENESIS, 1989, 4 (04) :286-291