STAT3 activation: A key factor in tumor immunoescape.

JAK-STAT Pub Date : 2013-01-01 DOI:10.4161/jkst.23010
Cédric Rébé, Frédérique Végran, Hélène Berger, François Ghiringhelli
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引用次数: 135

Abstract

Cancer growth is controlled by cancer cells (cell intrinsic phenomenon), but also by the immune cells in the tumor microenvironment (cell extrinsic phenomenon). Thus cancer progression is mediated by the activation of transcription programs responsible for cancer cell proliferation, but also induced proliferation/activation of immunosuppressive cells such as Th17, Treg or myeloid derived suppressor cells (MDSCs). One of the key transcription factors involved in these pathways is the signal transducer and activator of transcription 3 (STAT3). In this review we will focus on STAT3 activation in immune cells, and how it impacts on tumor progression.

Abstract Image

STAT3激活:肿瘤免疫逃逸的关键因素。
肿瘤生长受癌细胞控制(细胞内禀现象),也受肿瘤微环境中的免疫细胞控制(细胞外禀现象)。因此,癌症的进展是由负责癌细胞增殖的转录程序的激活介导的,但也会诱导免疫抑制细胞(如Th17, Treg或髓源性抑制细胞(MDSCs))的增殖/激活。参与这些途径的关键转录因子之一是转录3的信号转导和激活因子(STAT3)。在这篇综述中,我们将重点关注免疫细胞中的STAT3激活,以及它如何影响肿瘤进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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