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c-Myc Stimulates Cell Invasion by Inhibiting FBX8 Function

Authors
Cho, Hyun JungOh, Yun JeongKwon, JunhyeKwon, Jae YoungKim, Kyung-SooKim, Hongtae
Issue Date
Oct-2010
Publisher
KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
Keywords
c-Myc; cell invasion; FBX8; tumorigenesis; ubiquitination
Citation
MOLECULES AND CELLS, v.30, no.4, pp 355 - 362
Pages
8
Journal Title
MOLECULES AND CELLS
Volume
30
Number
4
Start Page
355
End Page
362
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/13122
DOI
10.1007/s10059-010-0134-8
ISSN
1016-8478
0219-1032
Abstract
c-Myc is a cellular onco-protein and a transcriptional activator important for cell growth, cell division, and tumorigenesis. Despite all that is known of its function, the mechanism of how c-Myc contributes to tumorigenesis is unclear. To gain insight into the mechanism through which c-Myc protein exerts its oncogenic activity, we performed large-scale, tandem repeat affinity purification and identified the F box only protein 8 (FBX8), an F-box and Sec7 domain-containing protein, as a novel Myc-binding protein. The c-Myc/FBX8 interaction was mediated by the c-Myc box II (MBII) region. We also confirmed that Myc protein overexpression in 293T cells affected FBX8 cellular translocation and led to recovery from FBX8-mediated inhibition of ADP-ribosylation factor 6 (ARF6) function during cell invasion. Together, these results suggest that FBX8 is a novel c-Myc binding protein and that c-Myc induces cell invasive activity through the inhibition of FBX8 effects on ARF6 function during cell invasion.
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