Mechanisms of Non-canonical Signaling in Health and Disease: Diversity to Take Therapy up a Notch?

被引:19
作者
Alfred, Victor [1 ]
Vaccari, Thomas [1 ,2 ]
机构
[1] IFOM IEO Campus, Ist FIRC Oncol Mol, IFOM, Milan, Italy
[2] Univ Milan, Dipartimento Biosci, Milan, Italy
来源
MOLECULAR MECHANISMS OF NOTCH SIGNALING | 2018年 / 1066卷
关键词
Drosophila melanogaster; Ligand-independent signaling; mTOR/Akt signaling; Non-canonical activation; NF-kappa B signaling; Notch signaling; Wnt/beta-catenin signaling; AMYLOID PRECURSOR PROTEIN; NEURAL CREST FORMATION; C2 DOMAIN PROTEIN; OF-DELTEX GENE; GAMMA-SECRETASE; INTRACELLULAR DOMAIN; DOWN-SYNDROME; RBP-J; ENDOCYTIC TRAFFICKING; CELL-DIFFERENTIATION;
D O I
10.1007/978-3-319-89512-3_9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-canonical Notch signaling encompasses a wide range of cellular processes, diverging considerably from the established paradigm. It can dispense of ligand, proteolytic or nuclear activity. Non-canonical Notch signaling events have been studied mostly in the fruit fly Drosophila melanogaster, the organism in which Notch was identified first and a powerful model for understanding signaling outcomes. However, non-canonical events are ill-defined and their involvement in human physiology is not clear, hampering our understanding of diseases arising from Notch signaling alterations. At a time in which therapies based on specific targeting of Notch signaling are still an unfulfilled promise, detailed understanding of non-canonical Notch events might be key to devising more specific and less toxic pharmacologic options. Based on the blueprint of non-canonical signaling in Drosophila, here, we review and rationalize current evidence about non-canonical Notch signaling. Our effort might inform Notch biologists developing new research avenues and clinicians seeking future treatment of Notch-dependent diseases.
引用
收藏
页码:187 / 204
页数:18
相关论文
共 137 条
[21]   Visualization of APP dimerization and APP-Notch2 heterodimerization in living cells using bimolecular fluorescence complementation [J].
Chen, CD ;
Oh, SY ;
Hinman, JD ;
Abraham, CR .
JOURNAL OF NEUROCHEMISTRY, 2006, 97 (01) :30-43
[22]   Lethal giant discs, a novel C2-domain protein, restricts notch activation during endocytosis [J].
Childress, Jennifer L. ;
Acar, Melih ;
Tao, Chunyao ;
Haider, Georg .
CURRENT BIOLOGY, 2006, 16 (22) :2228-2233
[23]   Dishevelled limits Notch signalling through inhibition of CSL [J].
Collu, Giovanna M. ;
Hidalgo-Sastre, Ana ;
Acar, Ahmet ;
Bayston, Laura ;
Gildea, Clara ;
Leverentz, Michael K. ;
Mills, Christopher G. ;
Owens, Thomas W. ;
Meurette, Olivier ;
Dorey, Karel ;
Brennan, Keith .
DEVELOPMENT, 2012, 139 (23) :4405-4415
[24]  
Cornell M, 1999, GENETICS, V152, P567
[25]   Numb Localizes at Endosomes and Controls the Endosomal Sorting of Notch after Asymmetric Division in Drosophila [J].
Couturier, Lydie ;
Mazouni, Khallil ;
Schweisguth, Francois .
CURRENT BIOLOGY, 2013, 23 (07) :588-593
[26]   Drosophila Ndfip is a novel regulator of Notch signaling [J].
Dalton, H. E. ;
Denton, D. ;
Foot, N. J. ;
Ho, K. ;
Mills, K. ;
Brou, C. ;
Kumar, S. .
CELL DEATH AND DIFFERENTIATION, 2011, 18 (07) :1150-1160
[27]   CC2D1A and CC2D1B regulate degradation and signaling of EGFR and TLR4 [J].
Deshar, Rakesh ;
Cho, Eun-Bee ;
Yoon, Sungjoo Kim ;
Yoon, Jong-Bok .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 480 (02) :280-287
[28]  
DIEDERICH RJ, 1994, DEVELOPMENT, V120, P473
[29]   Su(dx) E3 ubiquitin ligase-dependent and -independent functions of Polychaetoid, the Drosophila ZO-1 homologue [J].
Djiane, Alexandre ;
Shimizu, Hideyuki ;
Wilkin, Marian ;
Mazleyrat, Sabine ;
Jennings, Martin D. ;
Avis, Johanna ;
Bray, Sarah ;
Baron, Martin .
JOURNAL OF CELL BIOLOGY, 2011, 192 (01) :189-200
[30]   Hey2 Regulation by FGF Provides a Notch-Independent Mechanism for Maintaining Pillar Cell Fate in the Organ of Corti [J].
Doetzlhofer, Angelika ;
Basch, Martin L. ;
Ohyama, Takahiro ;
Gessler, Manfred ;
Groves, Andrew K. ;
Segil, Neil .
DEVELOPMENTAL CELL, 2009, 16 (01) :58-69