首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Bromodichloromethane induces cell proliferation in different tissues of male F344 rats by suppression of E-cadherin expression via hypermethylation or transcriptional activation of c-myc and cyclin D1
【24h】

Bromodichloromethane induces cell proliferation in different tissues of male F344 rats by suppression of E-cadherin expression via hypermethylation or transcriptional activation of c-myc and cyclin D1

机译:溴二氯甲烷通过超甲基化或c-myc和cyclin D1的转录激活抑制E-钙粘着蛋白表达,从而诱导雄性F344大鼠不同组织中的细胞增殖

获取原文
获取原文并翻译 | 示例
           

摘要

The aim of this study was to investigate the mechanism of bromodichloromethane (BDCM) - induced cell proliferation in different tissues of male F344 rats. Rats were administered at doses of 0 and 100. mg/kg/day BDCM dissolved in corn oil by gavage for 5 days/week for 1, 4, 8 and 12 weeks. Then the colon, kidney and liver were collected. No histologic lesions were observed in the colon of rats exposed to BDCM, while there were mild nephrotoxicity and marginal hepatotoxicity related to BDCM treatment. Moreover, BDCM enhanced cell proliferation in the colon and kidney but not in the liver. In colons, hypermethylation in E-cadherin promoter might be associated with inhibition of mRNA and protein expression after 12 weeks of BDCM exposure. In kidneys, BDCM decreased E-cadherin mRNA expression, accompanying with transcriptional activation of c-myc and cyclin D1. However, suppression of E-cadherin mRNA and protein expression occurred in the absence of significant changes in DNA methylation. Therefore, suppression of E-cadherin expression via hypermethylation or transcriptional activation of c-myc and cyclin D1 may be involved in BDCM-induced cell proliferation in different tissues of male F344 rats.
机译:这项研究的目的是研究溴二氯甲烷(BDCM)诱导的雄性F344大鼠不同组织中细胞增殖的机制。通过管饲法以0和100. mg / kg /天的剂量将大鼠BDCM溶解在玉米油中,连续5天/周,持续1、4、8和12周。然后收集结肠,肾脏和肝脏。在暴露于BDCM的大鼠结肠中未观察到组织学损伤,而与BDCM治疗相关的轻度肾毒性和边缘性肝毒性。此外,BDCM可增强结肠和肾脏中的细胞增殖,但不会增强肝脏中的细胞增殖。在结肠中,暴露于BDCM 12周后,E-钙粘着蛋白启动子中的高甲基化可能与mRNA和蛋白表达的抑制有关。在肾脏中,BDCM降低E-cadherin mRNA表达,并伴随c-myc和cyclin D1的转录激活。但是,在DNA甲基化没有明显变化的情况下,抑制了E-cadherin mRNA和蛋白质表达。因此,通过过度甲基化或c-myc和细胞周期蛋白D1的转录激活抑制E-钙粘着蛋白表达可能与雄性F344大鼠不同组织中BDCM诱导的细胞增殖有关。

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