c-Myc Stimulates Cell Invasion by Inhibiting FBX8 Function
- Authors
- Cho, Hyun Jung; Oh, Yun Jeong; Kwon, Junhye; Kwon, Jae Young; Kim, Kyung-Soo; Kim, 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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