Presenilin modulates EGFR signaling and cell transformation by regulating the ubiquitin ligase Fbw7-Reference-Cited by-同舟云学术

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Presenilin modulates EGFR signaling and cell transformation by regulating the ubiquitin ligase Fbw7

Published:2010-03-08 Issue:20 Volume:29 Page:2950-2961
ISSN:0950-9232
Container-title:Oncogene
language:en
Short-container-title:Oncogene

Author:

Rocher-Ros V,Marco S,Mao J-H,Gines S,Metzger D,Chambon P,Balmain A,Saura C A

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Link

http://www.nature.com/articles/onc201057.pdf

Reference54 articles.

1. Alwan HA, van Zoelen EJ, van Leeuwen JE . (2003). Ligand-induced lysosomal epidermal growth factor receptor (EGFR) degradation is preceded by proteasome-dependent EGFR de-ubiquitination. J Biol Chem 278: 35781–35790.

2. Bhoumik A, Fichtman B, DeRossi C, Breitwieser W, Kluger HM, Davis S et al. (2008). Suppressor role of activating transcription factor 2 (ATF2) in skin cancer. Proc Natl Acad Sci USA 105: 1674–1679.

3. Blanpain C, Lowry W, Pasolli H, Fuchs E . (2006). Canonical notch signaling functions as a commitment switch in the epidermal lineage. Genes Dev 20: 3022–3035.

4. Chen ZJ, Sun LJ . (2009). Nonproteolytic functions of ubiquitin in cell signaling. Mol Cell 33: 275–286.

5. de Souza N, Vallier LG, Fares H, Greenwald I . (2007). SEL-2, the C. elegans neurobeachin/LRBA homolog, is a negative regulator of lin-12/Notch activity and affects endosomal traffic in polarized epithelial cells. Development 134: 691–702.

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4. Presenilin-Deficient Neurons and Astrocytes Display Normal Mitochondrial Phenotypes;Frontiers in Neuroscience;2021-01-22

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