...
首页> 外文期刊>Cell Growth & Differentiation: The Molecular Biology Journal of the American Association for Cancer Research >2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) modulates lactogenic hormone-mediated differentiation and gene expression in HC11 mouse mammary epithelial cells.
【24h】

2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) modulates lactogenic hormone-mediated differentiation and gene expression in HC11 mouse mammary epithelial cells.

机译:2-氨基-1-甲基-6-苯基咪唑并(4,5-b)吡啶(PhIP)在HC11小鼠乳腺上皮细胞中调节生激素的介导的分化和基因表达。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

2-Amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) is a mammary gland carcinogen in cooked meat. Using the HC11 mouse mammary epithelial cell line, a well-characterized model for hormone-mediated differentiation, we examined whether PhIP altered the expression of genes regulated by lactogenic hormones dexamethasone, insulin, and prolactin (DIP). When HC11-Lux cells (stably transfected with a beta-casein promoter luciferase construct) were cultured in DIP-containing medium, PhIP (100 microM) enhanced luciferase activity 11-fold over that observed in DIP medium alone. The effect of PhIP on augmenting luciferase activity was observed only when lactogenic hormones were included in the medium. Expression of the endogenous beta-casein gene was also higher in HC11 cells treated with PhIP in hormone-enriched medium. With the increased expression of beta-casein gene, the level of phospho-signal transducer and activator of transcription 5A (phospho-STAT5A), the transcription factor regulating beta-casein gene expression, was elevated in PhIP-exposed HC11 cells. AG490, a Janus kinase 2 (JAK2)-specific inhibitor, blocked the effect of PhIP on beta-casein gene expression. PhIP-treated cells also showed higher expression of Bcl-2 and lower expression of Bax, consistent with a possible antiapoptotic action of PhIP. The findings indicate that PhIP modulates lactogenic hormone-mediated gene expression in mammary epithelial cells, apparently via enhanced phosphorylation of STAT5A. The findings have implications for a novel mechanism of action of the mammary gland carcinogen PhIP.
机译:2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)是熟肉中的乳腺致癌物。使用HC11小鼠乳腺上皮细胞系(一种激素介导的分化非常成熟的模型),我们检查了PhIP是否改变了受乳原激素地塞米松,胰岛素和催乳激素(DIP)调控的基因的表达。当在含DIP的培养基中培养HC11-Lux细胞(稳定转染有β-酪蛋白启动子荧光素酶构建体)时,PhIP(100 microM)增强的荧光素酶活性是仅在DIP培养基中观察到的11倍。仅当培养基中包含生乳激素时,才能观察到PhIP对增强荧光素酶活性的影响。在富含激素的培养基中,用PhIP处理的HC11细胞中内源性β-酪蛋白基因的表达也较高。随着β-酪蛋白基因表达的增加,在暴露于PhIP的HC11细胞中,磷酸信号转导和转录激活因子5A(phospho-STAT5A)(调节β-酪蛋白基因表达的转录因子)的水平升高。 AG490是Janus激酶2(JAK2)特异性抑制剂,可阻断PhIP对β-酪蛋白基因表达的影响。 PhIP处理的细胞还显示出Bcl-2的较高表达和Bax的较低表达,这与PhIP的抗凋亡作用一致。这些发现表明,PhIP显然是通过增强STAT5A的磷酸化来调节乳腺上皮细胞中促乳激素介导的基因表达。这些发现对乳腺致癌物PhIP的新型作用机制具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号