巨/癌细胞相互作用通过核受体脱抑制通路调解激素抵抗
Ping Zhu1, Sung Hee Baek, Eliot M Bourk
1Howard Hughes Medical Institute, Department of Medicine, University of California, San Diego, School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
前列腺癌细胞和巨细胞触发选择性雄激素受体对抗剂/调节剂 (SARMs),以激活基因表达. 这种开关涉及一个保存的动机,TAB2,和炎症信号,将生殖功能与核受体反应联系起来.
科学领域:
- 分子生物学分子生物学
- 内分泌学 在内分泌学.
- 癌症研究 癌症研究
背景情况:
- 了解转录调节对于发育,平衡和荷尔蒙依赖性癌症至关重要.
- 选择性雄激素受体对抗剂/调节剂 (SARMs) 在治疗前列腺癌方面至关重要.
研究的目的:
- 阐明SARM功能从抑制到激活的开关背后的分子机制.
- 为了研究前列腺癌细胞/巨细胞相互作用在这个功能开关中的作用.
主要方法:
- 在性类固醇受体中研究了保留的N端 L/HX7LL 图案.
- 研究了TAB2对N-CoR核心压缩复合物的招募.
- 研究了炎症信号,MEKK1和N-CoR/HDAC复合体解雇的作用.
主要成果:
- 发现特定的前列腺癌细胞/巨细胞相互作用将SARM功能从抑制转变为激活.
- 确定了一种保存的L/HX7LL图案,它介导了TAB2对N-CoR的招募.
- 证明TAB2感知炎症信号,招募MEKK1来排斥N-CoR/HDAC,从而导致和雌激素受体基因的脱抑制.
结论:
- 一个保存的传感器机制将炎症和核受体连接体反应联系起来.
- 这种机制逆转了针对炎症的目标基因的性别类固醇依赖抑制.
- 这些发现将炎症信号通路与生殖生物学和癌症中的核受体功能联系起来.
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