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  4. CCN2 inhibits lung cancer metastasis through promoting DAPK-dependent anoikis and inducing EGFR degradation
 
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CCN2 inhibits lung cancer metastasis through promoting DAPK-dependent anoikis and inducing EGFR degradation

Journal
Cell Death and Differentiation
Journal Volume
20
Journal Issue
3
Pages
443-455
Date Issued
2013
Author(s)
Chang C.-C.
Yang M.-H.
BEEN-REN LIN  
Chen S.-T.
SZU-HUA PAN  
Hsiao M.
Lai T.-C.
SZE-KWAN LIN  
YUNG-MING JENG  
CHIA-YU CHU  
Chen R.-H.
PAN-CHYR YANG  
Eugene Chin Y.
Kuo M.-L.
DOI
10.1038/cdd.2012.136
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84873709117&doi=10.1038%2fcdd.2012.136&partnerID=40&md5=c42b79cb9310d665d0ddb133621eb505
https://scholars.lib.ntu.edu.tw/handle/123456789/434926
Abstract
CCN family protein 2 (CCN2), also known as connective tissue growth factor, is a secreting protein that modulates multiple cellular events. We previously demonstrated the metastasis-suppressive effect of CCN2 in lung cancer cells. In this study, we investigate the role of CCN2 in anoikis, a form of programmed cell death that is critical in suppressing cancer metastasis. CCN2 binds to the epidermal growth factor receptor (EGFR) and triggers ubiquitination by inhibiting the formation of the β-pix/Cbl complex, resulting in the degradation of EGFR. Binding of CCN2 to EGFR suppresses the phosphorylation of c-Src and extracellular signal-regulated kinase but increases the expression of death-associated protein kinase, which leads to anoikis. Overall, our findings provide evidence validating the use of CCN2 as an anti-metastatic therapy in lung cancer patients, and prospect a potential therapeutic synergy between CCN2 and the anti-EGFR antibody for the treatment of lung cancer. ? 2013 Macmillan Publishers Limited All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
Cbl protein; cetuximab; connective tissue growth factor; death associated protein kinase; epidermal growth factor receptor; mitogen activated protein kinase; p21 activated kinase interacting exchange factor; phosphatidylinositol 3 kinase; protein; protein kinase B; protein tyrosine kinase; unclassified drug; anoikis; article; cancer cell; carboxy terminal sequence; complex formation; controlled study; drug potentiation; human; human cell; lung cancer; metastasis inhibition; molecular model; priority journal; protein binding; protein degradation; protein domain; protein function; protein phosphorylation; ubiquitination
Publisher
Nature Publishing Group
Type
journal article

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