The Emerging Role of TRAF7 in Tumor Development

被引：67

作者：

Zotti, Tiziana ^{[1
]}

Scudiero, Ivan ^{[2
]}

Vito, Pasquale ^{[1
]}

Stilo, Romania ^{[1
]}

机构：

[1] Univ Sannio, Dipartimento Sci & Tecnol, Via Port Arsa 11, I-82100 Benevento, Italy

[2] Biogem Consortium, Ariano Irpino, Italy

来源：

JOURNAL OF CELLULAR PHYSIOLOGY | 2017年 / 232卷 / 06期

关键词：

NF-KAPPA-B; INACTIVATING MUTATIONS; SIGNALING PATHWAYS; SOMATIC MUTATIONS; GENOMIC ANALYSIS; C-MYB; GENE; MENINGIOMAS; PROMOTES; AKT1;

D O I：

10.1002/jcp.25676

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

The seven members of the tumor necrosis factor receptor (TNF-R)-associated factor (TRAF) family of intracellular proteins were originally discovered and characterized as signaling adaptor molecules coupled to the cytoplasmic regions of receptors of the TNF-R superfamily. Functionally, TRAFs act both as a scaffold and/or enzymatic proteins to regulate activation of mitogen-activated protein kinases (MAPKs) and transcription factors of nuclear factor-kappa B family (NF-kappa B). Given the wide variety of stimuli intracellularly conveyed by TRAF proteins, they are physiologically involved in multiple biological processes, including embryonic development, tissue homeostasis, and regulation of innate and adaptive immune responses. In the last few years, it has become increasingly evident the involvement of TRAF7, the last member of the TRAF family to be discovered, in the genesis and progression of several human cancers, placing TRAF7 in the spotlight as a novel tumor suppressor protein. In this paper, we review and discuss the literature recently produced on this subject. (C) 2016 The Authors. Journal of Cellular Physiology Published by Wiley Periodicals, Inc.

引用

页码：1233 / 1238

页数：6

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