Charles G D, Shiverick K T
Department of Pharmacology and Therapeutics, University of Florida, Gainesville, Florida 32610-0267, USA.
Biochem Biophys Res Commun. 1997 Sep 18;238(2):338-42. doi: 10.1006/bbrc.1997.7291.
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-1beta (IL-1beta) 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-1beta. 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.
本研究利用人子宫内膜腺癌细胞系(RL95-2),调查了2,3,7,8-四氯二苯并对二恶英(TCDD)在子宫生长中的潜在作用。蛋白质免疫印迹分析显示,在1 nM TCDD时细胞色素P4501A1(CYP1A1)诱导作用最强,但表皮生长因子受体(EGFR)蛋白水平无变化。Northern印迹分析表明,TCDD显著提高了CYP1A1和CYP1B1的稳态mRNA水平,在1 nM时达到最大值。TCDD在6小时时显著提高白细胞介素-1β(IL-1β)的mRNA水平,在36小时时显著提高尿激酶型纤溶酶原激活剂(uPA)和肿瘤坏死因子-α(TNF-α)的mRNA水平。核转录分析显示,TCDD显著增加CYP1A1的转录,但对CYP1B1、uPA或IL-1β无影响。这些结果表明,TCDD可差异调节子宫细胞中生长因子和细胞因子基因产物的表达,这可能有助于子宫疾病的发展。