The IL-17A/IL-17RA Axis Is Not Related to Overall Survival and Cancer Stem Cell Modulation in Pancreatic Cancer

Int J Mol Sci. 2020 Mar 23;21(6):2215. doi: 10.3390/ijms21062215.

Abstract

(1) Background: IL-17A accelerates pancreatic intraepithelial neoplasia (PanIN) progression. In this study, we examined whether IL-17A/IL-17RA promotes pancreatic ductal adenocarcinoma (PDAC) aggressiveness in terms of survival and cancer stem cell modulation. (2) Methods: In vitro, the wound-healing assay, the sphere formation assay, and flow cytometry were applied to assess cancer stem cell features. In vivo, pancreatic tumors were induced in C57BL/6 mice using electroporation with oncogenic plasmids (P53-/- R172H; KrasG12V). Anti-IL-17 antibodies were administered as immunotherapy. We analyzed IL-17A/IL-17RA related survival using publicly available transcriptomic data (n = 903). (3) Results: IL-17A/IL-17RA expression was not related to survival in PDAC patients. IL-17A neither induces stem cell markers nor increases sphere formation and cell motility in vitro. Blocking the IL-17A/IL-17RA axis in a murine pancreatic cancer model did not improve the survival of mice, but reduced the tumor burden slightly. (4) Conclusions: IL-17A does not promote stem cell expansion in PDAC cell lines. Blocking IL-17A/IL-17RA signaling does not interfere with pancreatic cancer development and progression and may not be considered as a promising monotherapy for PDAC.

Keywords: IL-17A; IL-17RA; cancer stem cell; immunotherapy; pancreatic cancer.

MeSH terms

  • Animals
  • Biomarkers
  • Carcinoma, Pancreatic Ductal / etiology
  • Carcinoma, Pancreatic Ductal / metabolism
  • Carcinoma, Pancreatic Ductal / mortality
  • Carcinoma, Pancreatic Ductal / pathology
  • Cell Line, Tumor
  • Disease Models, Animal
  • Disease Susceptibility
  • Humans
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism*
  • Mice
  • Molecular Targeted Therapy
  • Neoplastic Stem Cells / metabolism*
  • Pancreatic Neoplasms / etiology
  • Pancreatic Neoplasms / metabolism*
  • Pancreatic Neoplasms / mortality*
  • Pancreatic Neoplasms / pathology
  • Prognosis
  • Receptors, Interleukin-17 / genetics
  • Receptors, Interleukin-17 / metabolism*
  • Signal Transduction*
  • Xenograft Model Antitumor Assays

Substances

  • Biomarkers
  • IL17A protein, human
  • IL17RA protein, human
  • Interleukin-17
  • Receptors, Interleukin-17