Ras signaling through RASSF proteins

被引:76
作者
Donninger, Howard [1 ]
Schmidt, M. Lee [2 ]
Mezzanotte, Jessica [3 ]
Barnoud, Thibaut [3 ,4 ]
Clark, Geoffrey J. [2 ]
机构
[1] Univ Louisville, Dept Med, Louisville, KY 40202 USA
[2] Univ Louisville, Dept Pharmacoloxy & Toxicol, Louisville, KY 40202 USA
[3] Univ Louisville, JG Brown Canc Ctr, Mol Targets Program, Dept Biochem & Mol Genet, Louisville, KY 40202 USA
[4] Wistar Inst Anat & Biol, Program Mol & Cellular Oncogenesis, Philadelphia, PA 19104 USA
关键词
Ras; RASSF1A; NORE1A; Apoptosis; Signaling; p53; TUMOR-SUPPRESSOR GENE; CELL LUNG-CANCER; FREQUENT PROMOTER HYPERMETHYLATION; INCREASES GENOMIC INSTABILITY; K-RAS; EPIGENETIC INACTIVATION; ONCOGENIC RAS; HIPPO PATHWAY; RETINOBLASTOMA PROTEIN; DESTRUCTION COMPLEX;
D O I
10.1016/j.semcdb.2016.06.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There are six core RASSF family proteins that contain conserved Ras Association domains and may serve as Ras effectors. They lack intrinsic enzymatic activity and appear to function as scaffolding and localization molecules. While initially being associated with pro-apoptotic signaling pathways such as Bax and Hippo, it is now clear that they can also connect Ras to a surprisingly broad range of signaling pathways that control senescence, inflammation, autophagy, DNA repair, ubiquitination and protein acetylation. Moreover, they may be able to impact the activation status of pro-mitogenic Ras effector pathways, such as the Raf pathway. The frequent epigenetic inactivation of RASSF genes in human tumors disconnects Ras from pro-death signaling systems, enhancing Ras driven transformation and metastasis. The best characterized members are RASSF1A and RASSF5 (NORE1A). (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:86 / 95
页数:10
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