核受体E75/NR1D2通过整合Hippo和Notch通路促进瘤恶性转变
Xianping Wang1,2, Yifan Guo3,4, Peng Lin3,4
1Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, 310024, Zhejiang, China. wangxianping@westlake.edu.cn.
The EMBO journal
|November 8, 2024
概括
激素治疗的耐药性驱动瘤恶性病变. 过度表达E75核受体整合Hippo和Notch通路,促进癌症的进展,这种发现在哺乳动物中得到保护.
科学领域:
- 内分泌学 在内分泌学.
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 激素治疗耐药性是癌症的主要临床挑战.
- 将类固醇激素信号抑制与瘤恶性病变联系在一起的机制尚不清楚.
研究的目的:
- 为了研究类固醇激素信号在瘤恶性瘤中的作用.
- 通过激素抑制来确定驱动瘤进展的分子机制.
主要方法:
- 在Drosophila恶性上皮瘤中对ecdysone信号的分析.
- 全基因组DNA结合概况和生物化学分析.
- 在质母细胞瘤模型中,NR1D2 (哺乳动物E75同类) 的耗尽.
主要成果:
- 在恶性瘤中减少了ecdysone信号传递.
- E75过度表达通过整合Hippo和Notch途径促进恶性转变.
- NR1D2 枯竭抑制了Hippo和Notch目标基因的激活,阻碍了质母细胞瘤的进展.
结论:
- 激素抑制通过一种新的机制促进瘤恶性.
- 在瘤进展过程中,E75/NR1D2在整合Hippo和Notch途径方面发挥着保留作用.
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