| Literature DB >> 25242044 |
Svetlana A Fayngerts1, Jianping Wu2, Camilla L Oxley3, Xianglan Liu4, Anastassios Vourekas1, Terry Cathopoulis1, Zhaojun Wang1, Jian Cui4, Suxia Liu4, Honghong Sun1, Mark A Lemmon3, Lining Zhang4, Yigong Shi5, Youhai H Chen6.
Abstract
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 4,5-bisphosphate 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.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25242044 PMCID: PMC4198483 DOI: 10.1016/j.ccr.2014.07.025
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743