Interleukin-6 and insulin-like growth factor-1 synergistically promote the progression of NSCLC

Autoimmunity. 2018 Dec;51(8):399-407. doi: 10.1080/08916934.2018.1550079. Epub 2019 Jan 3.

Abstract

The signaling pathways of interleukin-6 (IL-6) and insulin-like growth factor 1 (IGF-1) play an important role in the progression of lung cancer, and this study aimed to explore whether they can synergistically promote the progression of non-small cell lung cancer (NSCLC). We found that IL-6, glycoprotein 130 (GP130), IGF-1 and IGF-1R were highly expressed in NSCLC (p = .000), and there was the correlation between GP130, IGF-1, and IGF-1R (p < .01). The overall survival of patients with the co-expression of GP130 and IGF-1R was significantly shorter (p = .0360). Co-stimulation of IL-6 and IGF-1 resulted in significantly enhanced in cell proliferation, (p < .05), invasion (p < .05), cycle (p < .05), apoptosis (p < .05), and the expression of signal molecules (GP130, IGF-1R, p-AKT, and p-ERK1/2) (all p < .05) in NSCLC cells. This experiment revealed that IL-6 and IGF-1 can synergistically promote the progression of NSCLC. The high expression of GP130 and IGF-1R is an independent risk factor for poor prognosis patients, and it is helpful to find a more accurate target for targeted therapy in NSCLC.

Keywords: Interleukin-6; Non-small cell lung cancer; insulin-like growth factor 1; signaling pathways; tissue microarray-immunohistochemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / immunology
  • Carcinoma, Non-Small-Cell Lung / mortality
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Cell Line, Tumor
  • Cell Movement / immunology
  • Cell Proliferation
  • Cytokine Receptor gp130 / immunology
  • Cytokine Receptor gp130 / metabolism
  • Disease Progression
  • Humans
  • Insulin-Like Growth Factor I / immunology
  • Insulin-Like Growth Factor I / metabolism*
  • Interleukin-6 / immunology
  • Interleukin-6 / metabolism*
  • Lung / immunology
  • Lung / pathology
  • Lung Neoplasms / immunology
  • Lung Neoplasms / mortality
  • Lung Neoplasms / pathology*
  • Neoplasm Invasiveness / immunology
  • Neoplasm Invasiveness / pathology
  • Prognosis
  • Receptor, IGF Type 1
  • Receptors, Somatomedin / immunology
  • Receptors, Somatomedin / metabolism
  • Survival Analysis

Substances

  • IGF1 protein, human
  • IGF1R protein, human
  • IL6 protein, human
  • IL6ST protein, human
  • Interleukin-6
  • Receptors, Somatomedin
  • Cytokine Receptor gp130
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1