| Literature DB >> 27505671 |
Yanfang Liu1, Yan Gu1, Yanmei Han1, Qian Zhang1, Zhengping Jiang1, Xiang Zhang1, Bo Huang2, Xiaoqing Xu2, Jianming Zheng3, Xuetao Cao4.
Abstract
The pre-metastatic niche educated by primary tumor-derived elements contributes to cancer metastasis. However, the role of host stromal cells in metastatic niche formation and organ-specific metastatic tropism is not clearly defined. Here, we demonstrate that lung epithelial cells are critical for initiating neutrophil recruitment and lung metastatic niche formation by sensing tumor exosomal RNAs via Toll-like receptor 3 (TLR3). TLR3-deficient mice show reduced lung metastasis in the spontaneous metastatic models. Mechanistically, primary tumor-derived exosomal RNAs, which are enriched in small nuclear RNAs, activate TLR3 in lung epithelial cells, consequently inducing chemokine secretion in the lung and promoting neutrophil recruitment. Identification of metastatic axis of tumor exosomal RNAs and host lung epithelial cell TLR3 activation provides potential targets to control cancer metastasis to the lung.Entities:
Keywords: TLR3; alveolar epithelial cell; exosomal RNA; metastasis; pre-metastatic niche
Mesh:
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Year: 2016 PMID: 27505671 DOI: 10.1016/j.ccell.2016.06.021
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743