IFN-γ induces cell growth inhibition by Fas-mediated apoptosis:: Requirement of STAT1 protein for up-regulation of Fas and FasL expression

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作者
Xu, XL
Fu, XY
Plate, J
Chong, ASF
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Gen Surg, Chicago, IL 60612 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Med, Chicago, IL 60612 USA
[3] Rush Presbyterian St Lukes Med Ctr, Dept Immunol Microbiol, Chicago, IL 60612 USA
[4] Yale Univ, Sch Med, Dept Pathol, New Haven, CT USA
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The mechanism by which IFN-gamma inhibits tumor cell growth has not been fully understood. Here we report that IFN-gamma up-regulated the expression of Fas and Fas ligand (FasL) on HT29 cells, a human colon adenocarcinoma cell line, and subsequently induced apoptosis of these cells. The kinetics of cell death in IFN-gamma-treated HT29 cells paralleled the increase in the levels of Fas and Fast expression. We further show that IFN-gamma up-regulated the expression of Fas and Fast in STAT1-transfected U3A cells but not in STAT1-deficient U3A cells. Correspondingly, IFN-gamma induced cell death in STAT1-transfected U3A cells hut not in STAT1-deficient U3A cells. IFN-gamma-induced cell death was inhibited by caspase-1 inhibitors. Our results suggest that cell growth inhibition by IFN-gamma is due to apoptosis mediated by Fas and Fast interaction.
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页码:2832 / 2837
页数:6
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