Suppression of insulin-induced AP-1 transactivation by menin accompanies inhibition of C-FOS induction

被引:13
作者
Yumita, WR [1 ]
Ikeo, Y [1 ]
Yamauchi, K [1 ]
Sakurai, A [1 ]
Hashizume, K [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Aging Med & Geriatr, Matsumoto, Nagano 3908621, Japan
关键词
MEN1; gene; multiple endocrine neoplasia type 1; endocrine tumor; tumor suppressor; signal transduction;
D O I
10.1002/ijc.10885
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The translation product of the MEN1 gene, menin, has been reported to suppress JunD-mediated activator protein-1 (AP-1) transactivation and inhibit Ras-mediated tumor formation, but its molecular mechanisms and physiologic significance have been poorly elucidated. To better understand the function of menin as a tumor suppressor, we examined the effect of menin on physiologically induced AP-1 activity. Overexpression of menin strongly suppressed insulin-induced AP-1 activity in CHO-IR cells, which express high levels of insulin receptor. We found that menin suppressed c-Fos induction at the transcriptional level, although that cannot explain the entire mechanism of AP-1 suppression by menin. Menin did not alter the expression levels of AP-1 proteins except c-Fos, phosphorylation of c-Jun and JunD and DNA binding properties of AP-1 proteins. Suppression of AP-1 activation by menin may be exerted through 2 independent mechanisms, direct inhibition on AP-1-mediated transcription and suppression of c-Fos induction. The molecular mechanism of inhibition of AP-1 function by menin needs further elucidation. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:738 / 744
页数:7
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