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内皮TLR3–SLIT2信号轴的肿瘤激活可驱动转移
作者:小柯机器人 发布时间:2020/10/4 22:49:14

2020年9月30日《自然》杂志在线发表了美国洛克菲勒大学Sohail F. Tavazoie小组的最新成果,他们发现,内皮TLR3–SLIT2信号轴的肿瘤激活可驱动转移。

研究人员使用乳腺癌和肺癌的小鼠模型研究内皮细胞在癌症传播中是否也具有积极的“指导性”作用。研究人员从高度和不良转移肿瘤中纯化了基因标记的内皮核糖体及其相关的转录本。深度测序表明,转移性肿瘤诱导了轴突指导基因Slit2在内皮中的表达,从而在内皮(高Slit2表达)和肿瘤(低Slit2表达)区室之间建立了差异表达。内皮来源的SLIT2蛋白及其受体ROBO1促进了癌细胞向内皮细胞的迁移和血管的浸润。在乳腺癌和肺癌的小鼠模型中,敲除内皮Slit2抑制了转移扩散。相反,肿瘤Slit2的缺失增强了转移进程。
 
研究人员确定了源自肿瘤细胞的双链RNA作为上游信号,通过作用于RNA感应受体TLR3来诱导内皮SLIT2的表达。进而,一组内源性逆转录病毒元件RNA在转移细胞中被上调并在细胞外被检测到。因此,癌细胞会选择先天RNA感应来诱导内皮中的趋化性信号传导途径,从而驱动内渗和转移。
 
这些发现表明,内皮细胞在驱动转移性扩散中具有直接的指导作用,并证明单个基因(Slit2)可以根据其细胞来源促进或抑制癌症的进展。
 
据悉,血管通过提供营养和氧气来支持肿瘤,同时还充当着传播癌症的渠道。
 
附:英文原文

Title: Tumoural activation of TLR3–SLIT2 axis in endothelium drives metastasis

Author: Bernardo Tavora, Tobias Mederer, Kai J. Wessel, Simon Ruffing, Mahan Sadjadi, Marc Missmahl, Benjamin N. Ostendorf, Xuhang Liu, Ji-Young Kim, Olav Olsen, Alana L. Welm, Hani Goodarzi, Sohail F. Tavazoie

Issue&Volume: 2020-09-30

Abstract: Blood vessels support tumours by providing nutrients and oxygen, while also acting as conduits for the dissemination of cancer1. Here we use mouse models of breast and lung cancer to investigate whether endothelial cells also have active ‘instructive’ roles in the dissemination of cancer. We purified genetically tagged endothelial ribosomes and their associated transcripts from highly and poorly metastatic tumours. Deep sequencing revealed that metastatic tumours induced expression of the axon-guidance gene Slit2 in endothelium, establishing differential expression between the endothelial (high Slit2 expression) and tumoural (low Slit2 expression) compartments. Endothelial-derived SLIT2 protein and its receptor ROBO1 promoted the migration of cancer cells towards endothelial cells and intravasation. Deleting endothelial Slit2 suppressed metastatic dissemination in mouse models of breast and lung cancer. Conversely, deletion of tumoural Slit2 enhanced metastatic progression. We identified double-stranded RNA derived from tumour cells as an upstream signal that induces expression of endothelial SLIT2 by acting on the RNA-sensing receptor TLR3. Accordingly, a set of endogenous retroviral element RNAs were upregulated in metastatic cells and detected extracellularly. Thus, cancer cells co-opt innate RNA sensing to induce a chemotactic signalling pathway in endothelium that drives intravasation and metastasis. These findings reveal that endothelial cells have a direct instructive role in driving metastatic dissemination, and demonstrate that a single gene (Slit2) can promote or suppress cancer progression depending on its cellular source. Expression of the axon-guidance gene Slit2 in endothelium, induced by endothelial sensing of tumour-derived double-stranded RNA, promotes metastatic dissemination in mouse models of breast and lung cancer.

DOI: 10.1038/s41586-020-2774-y

Source: https://www.nature.com/articles/s41586-020-2774-y

期刊信息

Nature:《自然》,创刊于1869年。隶属于施普林格·自然出版集团,最新IF:43.07
官方网址:http://www.nature.com/
投稿链接:http://www.nature.com/authors/submit_manuscript.html