KRASG12 mutant induces the release of the WSTF/NRG3 complex, and contributes to an oncogenic paracrine signaling pathway

Oncotarget. 2016 Aug 16;7(33):53153-53164. doi: 10.18632/oncotarget.10625.

Abstract

It remains unclear how the signals of mutant KRASG12 in the transformed cells spread to the surrounding non-mutated cells and changes the microenvironment to promote tumor formation. We identified that Williams-Beuren syndrome transcription factor (WSTF), a non-secretory protein, was released in complex with secretory protein-neuregulin-3 (NRG3). The KRASG12 mutant activates the transcription of NRG3. The WSTF/NRG3 in extracellular space could activate oncogenic pathways in normal colon cells carrying wild type KRAS and endow them with the ability to express NRG3 and release WSTF/NRG3. Extracellular WSTF/NRG3 promotes the formation of colon tumors. Blockade of extracellular WSTF could restore cetuximab sensitivity of colon cancer cells with mutant KRAS. The appearance of WSTF/NRG3 in serum and urine correlates with a colon tumor carrying a KRASG12 mutant. In summary, our demonstration provides a new pathway to our understanding of the biological development of complex diseases.

Keywords: NRG3; RAS; WSTF; paracrine signaling.

MeSH terms

  • A549 Cells
  • Animals
  • Antineoplastic Agents, Immunological / pharmacology
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Cetuximab / pharmacology
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology
  • Epithelial Cells / metabolism
  • Female
  • Glycine / genetics
  • HeLa Cells
  • Humans
  • MCF-7 Cells
  • Mice, Inbred BALB C
  • Mutation, Missense*
  • Neuregulins / genetics*
  • Neuregulins / metabolism
  • Paracrine Communication / genetics*
  • Protein Binding
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • RNA Interference
  • Signal Transduction / genetics
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transplantation, Heterologous

Substances

  • Antineoplastic Agents, Immunological
  • BAZ1B protein, human
  • KRAS protein, human
  • NRG3 protein, human
  • Neuregulins
  • Transcription Factors
  • Proto-Oncogene Proteins p21(ras)
  • Cetuximab
  • Glycine