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γ干扰素通过Fas介导的凋亡诱导细胞生长抑制:STAT1蛋白对Fas和FasL表达上调的需求。

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

作者信息

Xu X, Fu X Y, Plate J, Chong A S

机构信息

Department of General Surgery, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612, USA.

出版信息

Cancer Res. 1998 Jul 1;58(13):2832-7.

PMID:9661898
Abstract

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 FasL expression. We further show that IFN-gamma up-regulated the expression of Fas and FasL in STAT1-transfected U3A cells but not in STAT1-deficient U3A cells. Correspondingly, IFN-gamma induced cell death in STAT1-transfected U3A cells but 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 FasL interaction.

摘要

γ干扰素抑制肿瘤细胞生长的机制尚未完全明确。在此我们报告,γ干扰素上调了人结肠腺癌细胞系HT29细胞上Fas及Fas配体(FasL)的表达,随后诱导这些细胞发生凋亡。经γ干扰素处理的HT29细胞的死亡动力学与Fas和FasL表达水平的增加相一致。我们进一步表明,γ干扰素上调了转染STAT1的U3A细胞中Fas和FasL的表达,但在STAT1缺陷的U3A细胞中则未上调。相应地,γ干扰素在转染STAT1的U3A细胞中诱导细胞死亡,但在STAT1缺陷的U3A细胞中则未诱导。γ干扰素诱导的细胞死亡被caspase-1抑制剂所抑制。我们的结果提示,γ干扰素对细胞生长的抑制是由于Fas和FasL相互作用介导的凋亡所致。

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