Clonorchis sinensis excretory-secretory products regulate migration and invasion in cholangiocarcinoma cells via extracellular signal-regulated kinase 1/2/nuclear factor-κB-dependent matrix metalloproteinase-9 expression

Int J Parasitol. 2017 Jan;47(1):51-59. doi: 10.1016/j.ijpara.2016.10.004. Epub 2016 Dec 3.

Abstract

Matrix metalloproteinase-9 plays an important role in the invasion and metastasis of various types of cancer cells. We have previously reported that excretory-secretory products from Clonorchis sinensis increases matrix metalloproteinase-9 expression. However, the regulatory mechanisms through which matrix metalloproteinase-9 expression affects cholangiocarcinoma development remain unclear. In the current study, we examined the potential role of excretory-secretory products in regulating the migration and invasion of various cholangiocarcinoma cell lines. We demonstrated that excretory-secretory products significantly induced matrix metalloproteinase-9 expression and activity in a concentration-dependent manner. Reporter gene and chromatin immunoprecipitation assays showed that excretory-secretory products induced matrix metalloproteinase-9 expression by enhancing the activity of nuclear factor-kappa B. Moreover, excretory-secretory products induced the degradation and phosphorylation of IκBα and stimulated nuclear factor-kappa B p65 nuclear translocation, which was regulated by extracellular signal-regulated kinase 1/2. Taken together, our findings indicated that the excretory-secretory product-dependent enhancement of matrix metalloproteinase-9 activity and subsequent induction of IκBα and nuclear factor-kappa B activities may contribute to the progression of cholangiocarcinoma.

Keywords: Cholangiocarcinoma; Clonorchis sinensis; Excretory–secretory products; Extracellular matrix; Matrix metalloproteinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bile Duct Neoplasms / metabolism
  • Bile Duct Neoplasms / parasitology*
  • Bile Duct Neoplasms / pathology
  • Cell Line, Tumor
  • Cholangiocarcinoma / metabolism
  • Cholangiocarcinoma / parasitology*
  • Cholangiocarcinoma / pathology
  • Clonorchiasis / metabolism*
  • Clonorchis sinensis / genetics
  • Clonorchis sinensis / immunology
  • Clonorchis sinensis / metabolism*
  • Cytokines / biosynthesis
  • Cytokines / immunology
  • Humans
  • MAP Kinase Signaling System
  • Male
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • Mitogen-Activated Protein Kinase 1 / metabolism*
  • Mitogen-Activated Protein Kinase 3 / metabolism*
  • NF-KappaB Inhibitor alpha / metabolism
  • NF-kappa B / drug effects*
  • NF-kappa B / metabolism
  • Neoplasm Metastasis
  • Phosphorylation
  • Rabbits

Substances

  • Cytokines
  • NF-kappa B
  • NF-KappaB Inhibitor alpha
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • MMP9 protein, human
  • Matrix Metalloproteinase 9