首页> 美国卫生研究院文献>iScience >Estrogen Induces Mammary Ductal Dysplasia via the Upregulation of Myc Expression in a DNA-Repair-Deficient Condition
【2h】

Estrogen Induces Mammary Ductal Dysplasia via the Upregulation of Myc Expression in a DNA-Repair-Deficient Condition

机译:雌激素通过在DNA修复缺陷状态下Myc表达的上调诱导乳腺导管发育异常

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

Mammary ductal dysplasia is a phenotype observed in precancerous lesions and early-stage breast cancer. However, the mechanism of dysplasia formation remains elusive. Here we show, by establishing a novel dysplasia model system, that estrogen, a female hormone, has the potential to cause mammary ductal dysplasia. We injected estradiol (E2), the most active form of estrogen, daily into scid mice with a defect in non-homologous end joining repair and observed dysplasia formation with cell proliferation at day 30. The protooncogene is a downstream target of estrogen signaling, and we found that its expression is augmented in mammary epithelial cells in this dysplasia model. Treatment with a Myc inhibitor reduced E2-induced dysplasia formation. Moreover, we found that isoflavones inhibited E2-induced dysplasia formation. Our dysplasia model system provides insights into the mechanistic understanding of breast tumorigenesis and the development of breast cancer prevention.
机译:乳腺导管发育不良是在癌前病变和早期乳腺癌中观察到的表型。但是,发育异常形成的机制仍然难以捉摸。在这里,我们通过建立新型的异型增生模型系统来表明,雌激素(一种女性激素)具有引起乳腺导管异型增生的潜力。我们将雌二醇最活跃的形式雌二醇(E2)每天注射到scid小鼠中,该小鼠在非同源末端连接修复中存在缺陷,并在第30天观察到发育异常形成并伴随细胞增殖。原癌基因是雌激素信号传导的下游靶标,并且我们发现,在这种发育异常模型中,其表达在乳腺上皮细胞中增加。用Myc抑制剂治疗可减少E2诱导的异型形成。此外,我们发现异黄酮抑制E2诱导的异型形成。我们的发育异常模型系统提供了对乳腺肿瘤发生的机理理解和预防乳腺癌发展的见识。

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