首页> 美国卫生研究院文献>Journal of Toxicologic Pathology >Enhanced Urinary Bladder Liver and Colon Carcinogenesis in Zucker Diabetic Fatty Rats in a Multiorgan Carcinogenesis Bioassay: Evidence for Mechanisms Involving Activation of PI3K Signaling and Impairment of p53 on Urinary Bladder Carcinogenesis
【2h】

Enhanced Urinary Bladder Liver and Colon Carcinogenesis in Zucker Diabetic Fatty Rats in a Multiorgan Carcinogenesis Bioassay: Evidence for Mechanisms Involving Activation of PI3K Signaling and Impairment of p53 on Urinary Bladder Carcinogenesis

机译:Zucker糖尿病患者尿膀胱肝和结肠癌的发生增强 多器官致癌生物测定中的肥胖大鼠:涉及机制的证据。 膀胱内PI3K信号的激活和p53的损伤 致癌作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

In the present study, modifying effects of diabetes on carcinogenesis induced in type 2 diabetes mellitus model Zucker diabetic fatty (ZDF) rats were investigated using a multiorgan carcinogenesis bioassay. Our re sults demonstrated enhancement of urinary bladder, colon and liver carcinogenesis in ZDF rats treated with five types of carcinogens (DMBDD). Elevated insulin and leptin and decreased adiponectin levels in the serum may be responsible for the high susceptibility of type 2 diabetes mellitus model rats to carcinogenesis in these organs. Possible mechanisms of increased susceptibility of diabetic rats to bladder carcinogenesis could be activation of the PI3K pathway and suppression of p53 in the urothelium in consequence of the above serum protein alterations.
机译:在本研究中,使用多器官致癌生物测定法研究了糖尿病对2型糖尿病模型Zucker糖尿病性脂肪(ZDF)大鼠诱导的致癌作用的改善作用。我们的研究结果表明,用五种致癌物(DMBDD)处理的ZDF大鼠的膀胱,结肠和肝癌发生能力增强。血清中胰岛素和瘦素的升高以及脂联素水平的降低可能是导致2型糖尿病模型大鼠对这些器官发生癌变的高度敏感性。糖尿病大鼠对膀胱癌发生的敏感性增加的可能机制可能是由于上述血清蛋白改变导致PI3K通路的激活和尿路上皮中p53的抑制。

著录项

相似文献

  • 外文文献
代理获取

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