Tumor Exosomal RNAs Promote Lung Pre-metastatic Niche Formation by Activating Alveolar Epithelial TLR3 to Recruit Neutrophils

Cancer Cell. 2016 Aug 8;30(2):243-256. doi: 10.1016/j.ccell.2016.06.021.

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.

Keywords: TLR3; alveolar epithelial cell; exosomal RNA; metastasis; pre-metastatic niche.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Carcinoma, Lewis Lung / genetics
  • Carcinoma, Lewis Lung / metabolism
  • Carcinoma, Lewis Lung / pathology
  • Epithelial Cells / pathology
  • Exosomes*
  • Humans
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Lung Neoplasms / secondary*
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / metabolism
  • Melanoma, Experimental / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neoplasm Metastasis
  • Neutrophil Infiltration / genetics*
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism*
  • RNA, Small Nuclear / genetics
  • RNA, Small Nuclear / metabolism
  • Toll-Like Receptor 3 / deficiency
  • Toll-Like Receptor 3 / genetics*
  • Toll-Like Receptor 3 / metabolism

Substances

  • RNA, Neoplasm
  • RNA, Small Nuclear
  • TLR3 protein, human
  • TLR3 protein, mouse
  • Toll-Like Receptor 3