ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells

被引:129
作者
Mousli, M
Hopfner, R
Abbady, AQ
Monté, D
Jeanblanc, M
Oudet, P
Louis, B
Bronner, C
机构
[1] Fac Pharm, INSERM, U392, F-67401 Illkirch Graffenstaden, France
[2] CNRS, UMR 7104, IGBMC, INSERM,U184, F-67404 Illkirch Graffenstaden, France
[3] Inst Pasteur, CNRS, UMR 8117, Inst Biol Lille, F-59021 Lille, France
[4] Ctr Pathol, F-67000 Strasbourg, France
关键词
ICBP90; topoisomerase II alpha; cancer; cell cycle; E2F; retinoblastoma protein;
D O I
10.1038/sj.bjc.6601068
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ICBP90 (Inverted CCAAT box Binding Protein of 90 kDa) is a recently identified nuclear protein that binds to one of the inverted CCAAT boxes of the topoisomerase IIalpha (TopoIIalpha) gene promoter. Here, we show that ICBP90 shares structural homology with several other proteins, including Np95, the human and mouse NIRF, suggesting the emergence of a new family of nuclear proteins. Towards elucidating the functions of this family, we analysed the expression of ICBP90 in various cancer or noncancer cell lines and in normal or breast carcinoma tissues. We found that cancer cell lines express higher levels of ICBP90 and TopoIIa than noncancer cell lines. By using cell-cycle phase-blocking drugs, we show that in primary cultured human lung fibroblasts, ICBP90 expression peaks at late G1 and during G2/M phases. In contrast, cancer cell lines such as HeLa, Jurkat and A549 show constant ICBP90 expression throughout the entire cell cycle. The effect of overexpression of E2F-1 is more efficient on ICBP90 and TopoIIa expression in noncancer cells (IMR90, WI38) than in cancer cells (U2OS, SaOs). Together, these results show that ICBP90 expression is altered in cancer cell lines and is upregulated by E2F-1 overexpression with an efficiency depending on the cancer status of the cell line.
引用
收藏
页码:120 / 127
页数:8
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