ADAM17 is required for EGF-R-induced intestinal tumors via IL-6 trans-signaling

J Exp Med. 2018 Apr 2;215(4):1205-1225. doi: 10.1084/jem.20171696. Epub 2018 Feb 22.

Abstract

Colorectal cancer is treated with antibodies blocking epidermal growth factor receptor (EGF-R), but therapeutic success is limited. EGF-R is stimulated by soluble ligands, which are derived from transmembrane precursors by ADAM17-mediated proteolytic cleavage. In mouse intestinal cancer models in the absence of ADAM17, tumorigenesis was almost completely inhibited, and the few remaining tumors were of low-grade dysplasia. RNA sequencing analysis demonstrated down-regulation of STAT3 and Wnt pathway components. Because EGF-R on myeloid cells, but not on intestinal epithelial cells, is required for intestinal cancer and because IL-6 is induced via EGF-R stimulation, we analyzed the role of IL-6 signaling. Tumor formation was equally impaired in IL-6-/- mice and sgp130Fc transgenic mice, in which only trans-signaling via soluble IL-6R is abrogated. ADAM17 is needed for EGF-R-mediated induction of IL-6 synthesis, which via IL-6 trans-signaling induces β-catenin-dependent tumorigenesis. Our data reveal the possibility of a novel strategy for treatment of colorectal cancer that could circumvent intrinsic and acquired resistance to EGF-R blockade.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM17 Protein / deficiency
  • ADAM17 Protein / metabolism*
  • Adenomatous Polyposis Coli / metabolism
  • Animals
  • Carcinogenesis / metabolism
  • Carcinogenesis / pathology
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology
  • Disease Models, Animal
  • ErbB Receptors / metabolism*
  • Gastrointestinal Microbiome
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Interleukin-6 / metabolism*
  • Intestinal Neoplasms / genetics
  • Intestinal Neoplasms / metabolism*
  • Intestinal Neoplasms / pathology*
  • Intestine, Small / pathology
  • Ki-67 Antigen / metabolism
  • Mice, Inbred C57BL
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Organoids / pathology
  • Prognosis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction*
  • Tumor Burden
  • beta Catenin / metabolism

Substances

  • Interleukin-6
  • Ki-67 Antigen
  • RNA, Messenger
  • STAT3 Transcription Factor
  • beta Catenin
  • ErbB Receptors
  • ADAM17 Protein