TIPE3 Is the Transfer Protein of Lipid Second Messengers that Promote Cancer

被引:108
作者
Fayngerts, Svetlana A. [1 ]
Wu, Jianping [2 ]
Oxley, Camilla L. [3 ]
Liu, Xianglan [4 ]
Vourekas, Anastassios [1 ]
Cathopoulis, Terry [1 ]
Wang, Zhaojun [1 ]
Cui, Jian [4 ]
Liu, Suxia [4 ]
Sun, Honghong [1 ]
Lemmon, Mark A. [3 ]
Zhang, Lining [4 ]
Shi, Yigong [2 ]
Chen, Youhai H. [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
[3] Univ Penn, Perelman Sch Med, Dept Biochem & Biophys, Philadelphia, PA 19104 USA
[4] Shandong Univ, Sch Med, Inst Immunol, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOSPHOINOSITIDE BINDING; NEGATIVE REGULATOR; STRUCTURAL BASIS; PATHWAY; PIP2;
D O I
10.1016/j.ccr.2014.07.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
More than half of human cancers have aberrantly upregulated phosphoinositide signals; yet how phospholipid signals are controlled during tumorigenesis is not fully understood. We report here that TIPE3 (TNFAIP8L3) is the transfer protein of phosphoinositide second messengers that promote cancer. High-resolution crystal structure of TIPE3 shows a large hydrophobic cavity that is occupied by a phospholipid-like molecule. TIPE3 preferentially captures and shuttles two lipid second messengers, i.e., phosphatidylinositol 4,5bisphosphate and phosphatidylinositol 3,4,5-trisphosphate, and increases their levels in the plasma membrane. Notably, human cancers have markedly upregulated TIPE3 expression. Knocking out TIPE3 diminishes tumorigenesis, whereas enforced TIPE3 expression enhances it in vivo. Thus, the function and metabolism of phosphoinositide second messengers are controlled by a specific transfer protein during tumorigenesis.
引用
收藏
页码:465 / 478
页数:14
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