研究生学术报告预告登记(开题、中期、答辩)

       为加强研究生学术交流活动,推进学术创新,特开通“研究生学术报告预告区”。我校研究生和教师可以在预告区及时发布和了解有关研究生学术报告的信息,届时参加。也可就某学术报告展开专题讨论与交流。

报告人: 祁永浩
学号: 1015213008
学院: 药物科学与技术学院
报告类型: 第一次学术报告
日期: 12 March 2016
时间: 3:20 PM
地点: 24楼A302
导师: 周立军
题目: Screening compounds that can bind to TRAF6 by computer-aided drug design
内容提要:

TRAF6, a unique member of the TRAF family, is an adaptor for the signals induced by the interleukin-1 receptor/Toll-like receptor (IL-1R/TLR) superfamily and plays a critical role in innate immune responses. The RING domain of TRAF6 functions together with the E2 Ubc13/Uev1A complex to mediate AKT and TAK1 activations. AKT has been shown to promote cell survival by growth factors against several apoptotic stimuli and possesses a significant role not only in tumor development but also in the tumor’s potential response to cancer treatment. On the other hand, TAK1, transforming growth factor β–activated kinase 1, also exerts a critical role in pro-inflammatory cytokine and TLR-mediated signaling pathways. The ubiquitin-activated TAK1 can phosphorylate IκB kinase (IKK) complex and p38, which leads to the activation of c-Jun N-terminal kinase (JNK), nuclear factor (NF)-κB, and MAPK signaling pathways.

So, if we can find the compound which can bind to TRAF6, it will inhibit the activation of AKT and TAK1. Therefore, the compound could inhibit the proliferation of tumor cell and induce the early apoptosis of the cells.

图片:
登记人: 祁永浩
登记时间: Friday, 20 April 2018, 11:04 AM