c-Myc Stimulates Cell Invasion by Inhibiting FBX8 Function

被引:16
作者
Cho, Hyun Jung [1 ]
Oh, Yun Jeong [1 ]
Kwon, Junhye [2 ]
Kwon, Jae Young [1 ]
Kim, Kyung-Soo [3 ]
Kim, Hongtae [1 ]
机构
[1] Sungkyunkwan Univ, Dept Biol Sci, Suwon 440746, South Korea
[2] Sookmyung Womens Univ, Dept Biol Sci, Seoul 140742, South Korea
[3] Catholic Univ Korea, Seoul St Marys Hosp, Dept Family Med, Coll Med, Seoul 137040, South Korea
关键词
c-Myc; cell invasion; FBX8; tumorigenesis; ubiquitination; ESSENTIAL COFACTOR; ACTIVATION; ARF6; TRANSFORMATION; ONCOPROTEINS; COMPLEX; RAC1;
D O I
10.1007/s10059-010-0134-8
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
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.
引用
收藏
页码:355 / 362
页数:8
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