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A CD47-associated super-enhancer links pro-inflammatory signalling to CD47 upregulation in breast cancer

机译:CD47相关的超级增强剂将促炎信号与乳腺癌中CD47的上调联系起来

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摘要

CD47 is a cell surface molecule that inhibits phagocytosis of cells that express it by binding to its receptor, SIRPα, on macrophages and other immune cells. CD47 is expressed at different levels by neoplastic and normal cells. Here, to reveal mechanisms by which different neoplastic cells generate this dominant ‘don't eat me' signal, we analyse the CD47 regulatory genomic landscape. We identify two distinct super-enhancers (SEs) associated with CD47 in certain cancer cell types. We show that a set of active constituent enhancers, located within the two CD47 SEs, regulate CD47 expression in different cancer cell types and that disruption of CD47 SEs reduces CD47 gene expression. Finally we report that the TNF-NFKB1 signalling pathway directly regulates CD47 by interacting with a constituent enhancer located within a CD47-associated SE specific to breast cancer. These results suggest that cancers can evolve SE to drive CD47 overexpression to escape immune surveillance.
机译:CD47是一种细胞表面分子,通过与巨噬细胞和其他免疫细胞上的受体SIRPα结合来抑制表达它的细胞的吞噬作用。肿瘤细胞和正常细胞以不同水平表达CD47。在这里,为了揭示不同的肿瘤细胞产生这种主要的“不要吃我”信号的机制,我们分析了CD47调控基因组格局。我们确定在某些癌细胞类型中与CD47相关的两个不同的超级增强子(SE)。我们显示,位于两个CD47 SE中的一组活性成分增强子,调节不同癌细胞类型中的CD47表达,并且CD47 SE的破坏降低了CD47基因的表达。最后,我们报告了TNF-NFKB1信号通路通过与位于特定于乳腺癌的CD47相关SE中的组成增强子相互作用而直接调节CD47。这些结果表明,癌症可以进化出SE来驱动CD47过表达,从而逃避免疫监视。

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