2,3,7,8-tetrachlorodibenzo-p-dioxin increases mRNA levels for interleukin-1 beta, urokinase plasminogen activator, and tumor necrosis factor-alpha in human uterine endometrial adenocarcinoma RL95-2 cells

被引:31
作者
Charles, GD [1 ]
Shiverick, KT [1 ]
机构
[1] UNIV FLORIDA, DEPT THERAPEUT & PHARMACOL, GAINESVILLE, FL 32610 USA
关键词
D O I
10.1006/bbrc.1997.7291
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
This study investigated the potential role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in uterine growth utilizing a human endometrial adenocarcinoma cell line (RL95-2), Western immunoblot analysis showed a maximal induction of cytochrome P4501A1 (CYP1A1) at 1 nM TCDD, but no change in epidermal growth factor receptor (EGFR) protein level, Northern blot analysis showed that TCDD significantly increased the steady state mRNA level of CYP1A1 and CYP1B1 which was maximal at 1 nM. TCDD significantly increased mRNA levels for interleukin-1 beta (IL-1 beta) by 6h, and for urokinase plasminogen activator (uPA) and tumor necrosis factor-alpha (TNF-alpha) by 36h, Nuclear runoff analysis showed that transcription of CYP1A1 was significantly increased by TCDD with no effect on CYP1B1, uPA or IL-1 beta, These results indicate that TCDD can differentially alter the expression of growth factor and cytokine gene products in uterine cells which may contribute to the promotion of uterine disease. (C) 1997 Academic Press.
引用
收藏
页码:338 / 342
页数:5
相关论文
共 34 条
[1]
[Anonymous], 1992, CURRENT PROTOCOLS MO
[2]
2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN INHIBITION OF 17-BETA-ESTRADIOL-INDUCED INCREASES IN RAT UTERINE EPIDERMAL GROWTH-FACTOR RECEPTOR-BINDING ACTIVITY AND GENE-EXPRESSION [J].
ASTROFF, B ;
ROWLANDS, C ;
DICKERSON, R ;
SAFE, S .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1990, 72 (03) :247-252
[3]
A comparison of cathepsin D levels in endometriotic tissue and in uterine endometrium [J].
Bergqvist, A ;
Ferno, M ;
Mattson, S .
FERTILITY AND STERILITY, 1996, 65 (06) :1130-1134
[4]
Promotion of endometriosis by 2,3,7,8-tetrachlorodibenzo-p-dioxin in rats and mice: Time-dose dependence and species comparison [J].
Cummings, AM ;
Metcalf, JL ;
Birnbaum, L .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 138 (01) :131-139
[5]
DMOWSKI WP, 1994, ACTA OBSTET GYN SCAN, V73, P7
[6]
Cytokines (IL-1 beta and TNF alpha) in relation to biochemical and immunological effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in rats [J].
Fan, F ;
Yan, BF ;
Wood, G ;
Viluksela, M ;
Rozman, KK .
TOXICOLOGY, 1997, 116 (1-3) :9-16
[7]
PLASMINOGEN ACTIVATORS IN ECTOPIC AND UTERINE ENDOMETRIUM [J].
FERNANDEZSHAW, S ;
MARSHALL, JM ;
HICKS, B ;
BARLOW, DH ;
STARKEY, PM .
FERTILITY AND STERILITY, 1995, 63 (01) :45-51
[8]
POSTTRANSCRIPTIONAL STABILIZATION OF UROKINASE PLASMINOGEN-ACTIVATOR MESSENGER-RNA BY 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN IN A HUMAN KERATINOCYTE CELL-LINE [J].
GAIDO, KW ;
MANESS, SC .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 133 (01) :34-42
[9]
GLEICHER N, 1994, ACTA OBSTET GYN SCAN, V73, P15
[10]
QUANTITATIVE-ANALYSIS OF EPIDERMAL GROWTH-FACTOR RECEPTOR GENE-EXPRESSION IN ENDOMETRIOSIS [J].
HUANG, JC ;
YEH, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (04) :1097-1101