首页> 美国卫生研究院文献>PLoS Clinical Trials >Lack of Ubiquitin Specific Protease 8 (USP8) Mutations in Canine Corticotroph Pituitary Adenomas
【2h】

Lack of Ubiquitin Specific Protease 8 (USP8) Mutations in Canine Corticotroph Pituitary Adenomas

机译:缺乏皮质激素特异性垂体腺瘤中的泛素特异性蛋白酶8(USP8)突变。

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

PurposeCushing’s disease (CD), also known as pituitary-dependent hyperadrenocorticism, is caused by adrenocorticotropic hormone (ACTH)-secreting pituitary tumours. Affected humans and dogs have similar clinical manifestations, however, the incidence of the canine disease is thousand-fold higher. This makes the dog an obvious model for studying the pathogenesis of pituitary-dependent hyperadrenocorticism. Despite certain similarities identified at the molecular level, the question still remains whether the two species have a shared oncogenetic background. Recently, hotspot recurrent mutations in the gene encoding for ubiquitin specific protease 8 (USP8) have been identified as the main driver behind the formation of ACTH-secreting pituitary adenomas in humans. In this study, we aimed to verify whether USP8 mutations also play a role in the development of such tumours in dogs.
机译:目的库欣病(CD)也称为垂体依赖性肾上腺皮质功能亢进症,是由分泌促肾上腺皮质激素(ACTH)的垂体肿瘤引起的。受影响的人和狗具有相似的临床表现,但是,犬病的发病率高出千倍。这使得该犬成为研究垂体依赖性肾上腺皮质功能亢进症发病机制的明显模型。尽管在分子水平上确定了某些相似性,但问题仍然是两个物种是否具有共同的致癌背景。最近,已确定编码泛素特异性蛋白酶8(USP8)的基因中的热点反复突变是人类分泌ACTH的垂体腺瘤形成的主要驱动力。在这项研究中,我们旨在验证USP8突变是否也在狗的此类肿瘤的发生中起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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