INHIBITION OF HIGH-DENSITY GROWTH ARREST IN HUMAN SQUAMOUS CARCINOMA-CELLS BY 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN (TCDD)

被引:29
作者
HEBERT, CD [1 ]
CAO, QL [1 ]
BIRNBAUM, LS [1 ]
机构
[1] UNIV N CAROLINA, CURRICULUM TOXICOL, CHAPEL HILL, NC 27599 USA
关键词
D O I
10.1093/carcin/11.8.1335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The highly toxic environmental contaminant 2,3,7,8-tetra-chlorodibenzo-p-dioxin (TCDD) is a potent carcinogen and tumor promoter, and affects cellular proliferation and differentiation both in vivo and in vitro. This report presents data showing that TCDD enhances the proliferation of two human squamous carcinoma cell lines in monolayer culture by inhibiting growth arrest at high cell density. SCC-15G and SCC-25 cells were treated with 0-100 nM TCDD in culture medium, and examined for changes in proliferation and differentiation. TCDD stimulated increases in cell number and DNA synthesis of both cell lines, and inhibited differentiation of SCC-15G cells in a dose-dependent manner. The minimum effective concentrations for increases in proliferation were 0.1 nM in SCC-15G cells and 1 nM in SCC-25G cells. The saturation density of SCC-15G cells grown in 10 nM TCDD was approximately double that of untreated controls, while the saturation density of SCC-25 cells was 50% above controls. TCDD-induced increases in proliferation were detectable only in cells exposed at subconfluent density, then assayed after control cultures had reached high-density growth arrest. There was no difference in cell number or DNA synthesis between control and TCDD-treated cultures when cells were both treated and assayed during the logarithmic phase of growth, nor in cultures treated after the cells had reached high density growth arrest. Therefore, TCDD-induced proliferation resulted from failure of treated cells to undergo normal density-dependent growth arrest rather than from direct mitogenic stimulation of the cells. Differentiation (envelope competence and keratin staining) of SCC-15G cells was inhibited by TCDD, despite the fact that in these cultures cell density was twice that of the controls. The sensitivity of SCC-15G cells to modulation of growth and differentiation by TCDD provides the basis for a model to examine the biological mechanisms of TCDD induced alterations in proliferation and differentiation of epidermal cells. © 1990 Oxford University Press.
引用
收藏
页码:1335 / 1342
页数:8
相关论文
共 39 条
[1]   THE OCCURRENCE AND FATE OF PCDDS AND PCDFS IN 5 BLEACHED KRAFT PULP AND PAPER-MILLS [J].
AMENDOLA, G ;
BARNA, D ;
BLOSSER, R ;
LAFLEUR, L ;
MCBRIDE, A ;
THOMAS, F ;
TIERNAN, T ;
WHITTEMORE, R .
CHEMOSPHERE, 1989, 18 (1-6) :1181-1188
[2]   OCCURRENCE OF PCDD AND PCDF IN DIFFERENT KINDS OF PAPER [J].
BECK, H ;
ECKART, K ;
MATHAR, W ;
WITTKOWSKI, R .
CHEMOSPHERE, 1988, 17 (01) :51-57
[3]  
BURKE MD, 1974, DRUG METAB DISPOS, V2, P583
[4]   TERATOLOGY STUDIES WITH 2,4,5-TRICHLOROPHENOXYACETIC ACID AND 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN [J].
COURTNEY, KD ;
MOORE, JA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1971, 20 (03) :396-&
[5]  
GIERTHY JF, 1984, TOXICOL APPL PHARM, V74, P91, DOI 10.1016/0041-008X(84)90274-6
[6]  
GREENLEE WF, 1987, REV BIOCHEM TOXICOL, P1
[7]  
GREENLEE WF, 1984, BANBURY REPORT 18, P435
[8]  
HARRIS M W, 1973, Environmental Health Perspectives, V5, P101, DOI 10.2307/3428118
[9]  
HEBERT CD, 1989, CANCER RES, V49, P3196
[10]   RELATIVE TOXICITY AND TUMOR-PROMOTING ABILITY OF 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN (TCDD), 2,3,4,7,8-PENTACHLORODIBENZOFURAN (PCDF), AND 1,2,3,4,7,8-HEXACHLORODIBENZOFURAN (HCDF) IN HAIRLESS MICE [J].
HEBERT, CD ;
HARRIS, MW ;
ELWELL, MR ;
BIRNBAUM, LS ;
HASKINS, EA ;
ALLEN, JD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 102 (02) :362-377