医学创新论坛
(第011期)
Title: Sag/Rbx2-Cullin RING ligase in cancer: from target identification to drug discovery
Speaker: Yi Sun(孙毅)
Institute of Translational Medicine
Zhejiang University School of Medicine
Host:Lin Mei
Chinese Institutes for Medical Research, Beijing
Time:9:15-10:30 a.m., Nov. 27, 2023 (Monday)
Location: Room 1322, North Tower, Basic Research Building, Capital Medical University (首都医科大学基础科研楼北楼1322会议室)
Abstract:
Cullin-RING ligase (CRL) is the largest family of E3 ubiquitin ligases, consisting of four components: 1) a scaffold protein cullin with 8 family members, 2) an adaptor protein, 3) a substrate-recognizing protein, and 4) a RING protein with two family members, RBX1 or RBX2 (also known as SAG). Upon activation by cullin neddylation, CRLs promote ubiquitylation and degradation of many key regulatory proteins, thus regulating a variety of biological processes, including cell cycle progression, signal transduction, responses to hypoxia, oxidative stress, DNA damage and repair, DNA replication, and tumorigenesis.
SAG/RBX2 is the RING component of CRLs, required for its activity. SAG is overexpressed in a number of human cancers, which is associated with poor survival of patients. We found that Sag deletion remarkably suppressed tumorigenesis in the lung, and pancreas, triggered by KrasG12D, and in the prostate, triggered by Pten loss, indicating that Sag is an oncogenic cooperating gene. We are actively engaged in drug discovery effort to find small molecule inhibitors that target SAG E3 ligase and neddylation for anticancer application. More details will be presented.
Selected Papers: