Cancer-associated fibroblasts promote the progression and chemoresistance of HCC by inducing IGF-1

Cell Signal. 2024 Dec:124:111378. doi: 10.1016/j.cellsig.2024.111378. Epub 2024 Sep 4.

Abstract

Crosstalk between cancer-associated fibroblasts (CAFs) and tumour cells plays a critical role in multiple cancers, including hepatocellular carcinoma (HCC). CAFs contribute to tumorigenesis by secreting growth factors, modifying the extracellular matrix, supporting angiogenesis, and suppressing antitumor immune responses. However, effect and mechanism of CAF-mediated promotion of hepatocellular carcinoma cells are still unclear. In study, we demonstrated CAFs promoted the proliferation and inhibited the apoptosis of HCC cells by secreting interleukin-6 (IL-6), which induced autocrine insulin-like growth factor-1 (IGF-1) in HCC. IGF-1 promoted the progression and chemoresistance of HCC. IGF-1 receptor (IGF-1R) inhibitor NT157 abrogated the effect of CAF-derived IL-6 and autocrine IGF-1 on HCC. Mechanistic studies revealed that NT157 decreased IL-6-induced IGF-1 expression by inhibiting STAT3 phosphorylation and led to IRS-1 degradation, which mediated the proliferation of tumour by activating AKT signalling in ERK-dependent manner. Inhibition of IGF-1R also enhanced the therapeutic effect of sorafenib on HCC, especially chemoresistant tumours. STATEMENT OF SIGNIFICANCE: Our study showed IL-6-IGF-1 axis played crucial roles in the crosstalk between HCC and CAFs, providing NT157 inhibited of STAT3 and IGF-1R as a new targeted therapy in combination with sorafenib.

Keywords: Hepatocellular carcinoma; Insulin-like growth factor 1 receptor; NT157; Sorafenib; cancer-associated fibroblasts.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cancer-Associated Fibroblasts* / metabolism
  • Cancer-Associated Fibroblasts* / pathology
  • Carcinoma, Hepatocellular* / metabolism
  • Carcinoma, Hepatocellular* / pathology
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • Disease Progression
  • Drug Resistance, Neoplasm* / drug effects
  • Humans
  • Imidazoles
  • Insulin-Like Growth Factor I* / metabolism
  • Interleukin-6* / metabolism
  • Liver Neoplasms* / metabolism
  • Liver Neoplasms* / pathology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pyrazines
  • Receptor, IGF Type 1* / metabolism
  • STAT3 Transcription Factor* / metabolism
  • Signal Transduction / drug effects
  • Sorafenib / pharmacology

Substances

  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1
  • Interleukin-6
  • STAT3 Transcription Factor
  • IGF1 protein, human
  • Sorafenib
  • 3-(8-amino-1-(2-phenylquinolin-7-yl)imidazo(1,5-a)pyrazin-3-yl)-1-methylcyclobutanol
  • IGF1R protein, human
  • Proto-Oncogene Proteins c-akt
  • Imidazoles
  • Pyrazines