Suppr超能文献

一个与 CD47 相关的超级增强子将促炎信号与乳腺癌中 CD47 的上调联系起来。

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

机构信息

Institute for Stem Cell Biology and Regenerative Medicine, and Ludwig Center for Cancer Stem Cell Research and Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.

Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.

出版信息

Nat Commun. 2017 Apr 5;8:14802. doi: 10.1038/ncomms14802.

Abstract

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.

摘要

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,抑制表达它的细胞被吞噬。肿瘤细胞和正常细胞的 CD47 表达水平不同。在这里,为了揭示不同肿瘤细胞产生这种显性“别吃我”信号的机制,我们分析了 CD47 的调控基因组景观。我们在某些癌细胞类型中鉴定出与 CD47 相关的两个不同的超级增强子(SE)。我们表明,位于两个 CD47 SE 内的一组活性组成增强子,在不同的癌细胞类型中调节 CD47 的表达,并且破坏 CD47 SE 会降低 CD47 基因的表达。最后,我们报告说 TNF-NFKB1 信号通路通过与位于乳腺癌特有的与 CD47 相关 SE 内的一个组成性增强子相互作用,直接调控 CD47。这些结果表明,癌症可以进化 SE 来驱动 CD47 过表达,从而逃避免疫监视。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb3e/5382276/94c6a8d7dd4c/ncomms14802-f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验