Interferon-alpha and transforming growth factor-β co-induce growth inhibition of human tumor cells

被引:20
作者
Foser, S.
Redwanz, I.
Ebeling, M.
Heizmann, C. W.
Certa, U. [1 ]
机构
[1] Hoffmann La Roche Ag, Roche Ctr Med Genom, CH-4070 Basel, Switzerland
[2] Hoffmann La Roche Ag, Dept Bioinformat, CH-4070 Basel, Switzerland
[3] Univ Zurich, Dept Pediat, Div Clin Chem & Biochem, CH-8032 Zurich, Switzerland
关键词
calcium signaling; cell proliferation; interferon-alpha; transforming growth factor-beta; S100; proteins;
D O I
10.1007/s00018-006-6256-7
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
A hallmark of resistance to type I interferons (IFNs) is the lack of antiproliferative responses. We show here that costimulation with IFN-alpha and transforming growth factor beta-1 (TGF-beta) potentiates antiproliferative activity in a sensitive (ME15) and resistant (D10) human melanoma cell line. A DNA microarray-based search for proliferation control genes involved that are cooperatively activated by IFN-alpha and TGF-beta, yielded 28 genes. Among these are the insulin-like growth factor-binding protein 3 (IGFBP3) and the calcium-binding protein S100A2; we demonstrate, that recombinant IGFBP3 protein is a potent growth inhibitor requiring TGF-beta activity. The antiproliferative activity of S100A2 is significantly enhanced by IFN-alpha in stably transfected ME15 or D10 cell lines. We show for the first time that IFN-alpha is a potent inducer of intracellular calcium release required for activation of S100A2. Our study provides a functional link between IFN-alpha and TGF-beta signaling and extends the function of IFN signaling to calcium-sensitive processes.
引用
收藏
页码:2387 / 2396
页数:10
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