EXPRESSION DYNAMICS OF TRANSFORMING PHENOTYPES IN X-IRRADIATED SYRIAN GOLDEN-HAMSTER EMBRYO CELLS

被引:22
作者
WATANABE, M
SUZUKI, K
机构
[1] Division of Radiation Biology, School of Medicine, Yokohama City University, Kanazawa-ku, Yokohama, 236
来源
MUTATION RESEARCH | 1991年 / 249卷 / 01期
基金
日本科学技术振兴机构;
关键词
MORPHOLOGICAL TRANSFORMATIONS; ANCHORAGE INDEPENDENCE; HGPRT MUTATION; SYRIAN GOLDEN HAMSTER;
D O I
10.1016/0027-5107(91)90133-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We investigated the dynamics of expression for morphological transformation, for anchorage-independently growing (Anch-) cells and for mutation at the hypoxanthine guanine phosphoribosyl transferase (HGPRT) locus in X-irradiated Syrian golden hamster embryo (SHE) cells. No Anch- cells were detected with 0-14 days of post-irradiation incubation before selection. No mutants at the HGPRT locus were detected with 0-5 days of post-irradiation incubation before selection. The maximum number of mutants for all doses was found after post-irradiation incubation for 8 days. On the other hand, the highest frequency of morphological transformants for all doses was detected with 0 days of post-irradiation incubation. The frequency of induction of morphological transformants increased with increasing dose. Then morphological transformants abruptly decreased with increasing lengths of post-irradiation incubation and no morphological transformants were detected with 14 days of post-irradiation incubation before selection (< 10(-4)). A large fraction of morphological transformants (more than 86%) was cloned with feeder cells and expressed more extensive phenotypes of malignant transformation, such as the acquisition of anchorage-independent growth, immortality in vitro and tumorigenicity during further subculturing.
引用
收藏
页码:71 / 80
页数:10
相关论文
共 42 条
[1]   COMPARISON OF THE FREQUENCY OF DIPHTHERIA-TOXIN AND THIOGUANINE RESISTANCE INDUCED BY A SERIES OF CARCINOGENS TO ANALYZE THEIR MUTATIONAL SPECIFICITIES IN DIPLOID HUMAN-FIBROBLASTS [J].
AUST, AE ;
DRINKWATER, NR ;
DEBIEN, K ;
MAHER, VM ;
MCCORMICK, JJ .
MUTATION RESEARCH, 1984, 125 (01) :95-104
[2]   ACTIVATION OF THE MOUSE CELLULAR HARVEY-RAS GENE IN CHEMICALLY-INDUCED BENIGN SKIN PAPILLOMAS [J].
BALMAIN, A ;
RAMSDEN, M ;
BOWDEN, GT ;
SMITH, J .
NATURE, 1984, 307 (5952) :658-660
[3]   ONCOGENE ACTIVATION IN CHEMICAL CARCINOGENESIS [J].
BALMAIN, A ;
BROWN, K .
ADVANCES IN CANCER RESEARCH, 1988, 51 :147-182
[4]   DIETHYLSTILBESTROL INDUCES NEOPLASTIC TRANSFORMATION WITHOUT MEASURABLE GENE MUTATION AT 2 LOCI [J].
BARRETT, JC ;
WONG, A ;
MCLACHLAN, JA .
SCIENCE, 1981, 212 (4501) :1402-1404
[5]   EVIDENCE FOR PROGRESSIVE NATURE OF NEOPLASTIC TRANSFORMATION INVITRO [J].
BARRETT, JC ;
TSO, POP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (08) :3761-3765
[6]  
BARRETT JC, 1987, MECHANISMS ENV CARCI, V2, P73
[7]  
BERENBLUM I, 1954, CANCER RES, V14, P471
[8]  
BIEDERMANN KA, 1987, CANCER RES, V47, P3815
[9]   IDENTIFICATION OF A CHROMOSOME THAT CONTROLS MALIGNANCY IN CHINESE-HAMSTER CELLS [J].
BLOCHSHTACHER, N ;
SACHS, L .
JOURNAL OF CELLULAR PHYSIOLOGY, 1977, 93 (02) :205-212
[10]   DISTINCTIVE TRANSFORMING GENES IN X-RAY-TRANSFORMED MAMMALIAN-CELLS [J].
BOREK, C ;
ONG, A ;
MASON, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (03) :794-798