首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >In vivo study on the effects of microcystin extracts on the expression profiles of proto-oncogenes (c-fos, c-jun and c-myc) in liver, kidney and testis of male Wistar rats injected i.v. with toxins
【24h】

In vivo study on the effects of microcystin extracts on the expression profiles of proto-oncogenes (c-fos, c-jun and c-myc) in liver, kidney and testis of male Wistar rats injected i.v. with toxins

机译:微囊藻毒素提取物对经静脉内注射的雄性Wistar大鼠肝脏,肾脏和睾丸中原癌基因(c-fos,c-jun和c-myc)表达谱的影响的体内研究。与毒素

获取原文
获取原文并翻译 | 示例
           

摘要

Microcystins (MCs) are a potent liver tumor promoter, possessing potent tumor-promoting activity and weak initiating activity. Proto-oncogenes are known to be involved in the tumor-promoting mechanisms of microcystin-LR. However, few data are available on the effects of MCs on proto-oncogenes in the whole animal. To investigate the effects of MCs on the expression profile of the proto-oncogenes in different organs, male Wistar rats were injected intravenously with microcystin extracts at a dose of86.7 mu g MC-LR eq/kg bw (MC-LR eq, MC-LR equivalents). mRNA levels of three proto-oncogenes c-fos, c-jun and c-myc in liver, kidney and testis were analyzed using quantitative real-time PCR at several time points post-injection. Significant induction ofthese genes at transcriptional level was observed in the three organs. In addition, the increase of mRNA expression of all three genes was much higher in liver than in kidney and testis. Meanwhile, the protein levels of c-Fos and c-Jun were investigatedby western blotting. Both proteins were induced in the three organs. However, elevations of protein levels were much lower than those of mRNA levels. These findings suggest that the expression of c-fos, c-jun and c-myc might be one possible mechanism for the tumor-promoting activity and initiating activity of microcystins.
机译:微囊藻毒素(MCs)是有效的肝肿瘤启动子,具有有效的促肿瘤活性和较弱的启动活性。已知原癌基因参与微囊藻毒素-LR的肿瘤促进机制。但是,关于MC对整个动物原癌基因的影响的数据很少。为了研究MC对不同器官中原癌基因表达谱的影响,向雄性Wistar大鼠静脉注射微囊藻毒素提取物,剂量为86.7μg MC-LR eq / kg bw(MC-LR eq,MC -LR等效)。在注射后的几个时间点,使用定量实时PCR分析了肝脏,肾脏和睾丸中三种原癌基因c-fos,c-jun和c-myc的mRNA水平。在三个器官中观察到这些基因在转录水平上的显着诱导。另外,肝脏中所有​​这三个基因的mRNA表达增加远高于肾脏和睾丸。同时,通过蛋白质印迹法研究了c-Fos和c-Jun的蛋白水平。两种蛋白质均在三个器官中被诱导。但是,蛋白质水平的升高远低于mRNA水平。这些发现表明,c-fos,c-jun和c-myc的表达可能是微囊藻毒素的促肿瘤活性和启动活性的一种可能机制。

著录项

相似文献

  • 外文文献
  • 中文文献
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