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人类癌细胞已经特异性地丧失了诱导由肿瘤坏死因子加β干扰素所引发的协同状态的能力。

Human cancer cells have specifically lost the ability to induce the synergistic state caused by tumor necrosis factor plus interferon-beta.

作者信息

Bartee Eric, McFadden Grant

机构信息

Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, 1600 SW Archer Road, R4-295, Gainesville, FL 32610, USA.

出版信息

Cytokine. 2009 Sep;47(3):199-205. doi: 10.1016/j.cyto.2009.06.006. Epub 2009 Jul 28.

Abstract

Tumor necrosis factor (TNF) and the members of the interferon (IFN) family are major inducible cytokines that function to counteract viral infections or cellular transformation. Recently, our lab has characterized a novel antiviral state which is induced in primary human fibroblasts by co-treatment with TNF plus IFNbeta. Here, we demonstrate that this synergistic state is both antiviral and cytostatic for primary human cells. Significantly, we observed that a wide spectrum of transformed human cancer cells have universally lost the ability to induce the TNF/IFNbeta synergistic state, as defined by three separate criteria. We hypothesize that the ability to induce the TNF/IFNbeta synergistic state is a unique feature of primary cells and is incompatible with cellular immortalization and/or transformation.

摘要

肿瘤坏死因子(TNF)和干扰素(IFN)家族成员是主要的诱导性细胞因子,其作用是对抗病毒感染或细胞转化。最近,我们实验室鉴定了一种新型抗病毒状态,该状态由TNF与IFNβ联合处理原代人成纤维细胞诱导产生。在此,我们证明这种协同状态对原代人细胞具有抗病毒和细胞生长抑制作用。值得注意的是,我们观察到,根据三个独立标准定义,多种转化的人类癌细胞普遍丧失了诱导TNF/IFNβ协同状态的能力。我们推测,诱导TNF/IFNβ协同状态的能力是原代细胞的独特特征,与细胞永生化和/或转化不相容。

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Tumor necrosis factor and interferon: cytokines in harmony.肿瘤坏死因子与干扰素:协同作用的细胞因子
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