Chromosomal aberrations in vitro induced by aneugens

被引:24
作者
Arni, P
Hertner, T
机构
[1] Novartis Crop Protection AG, P.O. Box
关键词
aneugen; structural chromosomal aberration; polyploidy; mitotic index; colcemid; colchicine; vincristine;
D O I
10.1016/S0027-5107(97)00111-5
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
Various aneugens were reported to induce structural chromosomal aberrations beside their influence on cell division and their aneugenic potential To assess, whether a relationship between disturbance of cell division and clastogenic potential exists, CHO cells were treated with the well-known aneugens colcemid, colchicine and vincristine and investigated for the induction of structural chromosomal aberrations, polyploid cells and alterations in mitotic index. At low and intermediate concentrations, all compounds induced polyploidy and an increase in mitotic index, but no structural aberrations at all. However, at high concentrations, colcemid and colchicine both induced numerous structural chromosomal aberrations in diploid cells. Colchicine was also clastogenic in tetraploid cells. Vincristine did not induce structural chromosomal aberrations in diploid cells, but in tetraploid cells. The clastogenic effects showed a clear-cut threshold with all three compounds. Furthermore, it was found that the tetraploid condition in CHO cells is generally accompanied by an increase in structural chromosomal aberrations, in vehicle controls as well as in cultures treated with the aneugens. Nevertheless, this study demonstrates that for the three aneugenic compounds tested, no direct relationship between compound induced disturbance of cell cycle and compound induced structural chromosomal aberration incidence exists. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:83 / 93
页数:11
相关论文
共 23 条
[1]  
AARDEMA MJ, UNPUB MUTATION RES
[2]   SYNOPSIS OF THE INVIVO RESULTS OBTAINED WITH THE 10 KNOWN OR SUSPECTED ANEUGENS TESTED IN THE CEC COLLABORATIVE STUDY [J].
ADLER, ID .
MUTATION RESEARCH, 1993, 287 (01) :131-137
[3]   2,4,6-TRICHLOROPHENOL (TCP) INDUCES CHROMOSOME BREAKAGE AND ANEUPLOIDY IN-VITRO [J].
ARMSTRONG, MJ ;
GALLOWAY, SM ;
ASHBY, J .
MUTATION RESEARCH, 1993, 303 (03) :101-108
[4]   MEASUREMENT OF LEVELS OF ANEUPLOIDY IN MAMMALIAN-CELLS USING A MODIFIED HYPOTONIC TREATMENT [J].
DANFORD, N .
MUTATION RESEARCH, 1984, 139 (03) :127-132
[5]   ANEUPLOIDY AND HEALTH RISK ASSESSMENT - CURRENT STATUS AND FUTURE-DIRECTIONS [J].
DELLARCO, VL ;
MAVOURNIN, KH ;
TICE, RR .
ENVIRONMENTAL MUTAGENESIS, 1985, 7 (03) :405-424
[6]   Indications for a threshold of chemically-induced aneuploidy in vitro in human lymphocytes [J].
Elhajouji, A ;
VanHummelen, P ;
KirschVolders, M .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1995, 26 (04) :292-304
[7]   CHROMOSOME-ABERRATIONS AND SISTER CHROMATID EXCHANGES IN CHINESE-HAMSTER OVARY CELLS - EVALUATIONS OF 108 CHEMICALS [J].
GALLOWAY, SM ;
ARMSTRONG, MJ ;
REUBEN, C ;
COLMAN, S ;
BROWN, B ;
CANNON, C ;
BLOOM, AD ;
NAKAMURA, F ;
AHMED, M ;
DUK, S ;
RIMPO, J ;
MARGOLIN, BH ;
RESNICK, MA ;
ANDERSON, B ;
ZEIGER, E .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1987, 10 :1-175
[8]   REPORT FROM WORKING GROUP ON IN-VITRO TESTS FOR CHROMOSOMAL-ABERRATIONS [J].
GALLOWAY, SM ;
AARDEMA, MJ ;
ISHIDATE, M ;
IVETT, JL ;
KIRKLAND, DJ ;
MORITA, T ;
MOSESSO, P ;
SOFUNI, T .
MUTATION RESEARCH, 1994, 312 (03) :241-261
[9]  
GEBHART E, 1969, MED KLIN, V51, P2366
[10]   Genetic toxicology of mitotic spindle inhibitors used as anticancer drugs [J].
KirschVolders, M ;
Parry, EM .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1996, 355 (1-2) :103-128