Fucoidan reduced the invasion of oral squamous cell carcinoma cells and modified their effects to macrophages

Med Oncol. 2017 Jan;34(1):9. doi: 10.1007/s12032-016-0858-1. Epub 2016 Dec 21.

Abstract

Fucoidan is a complex of polysaccharides showing antitumor and immunomodulation properties. Our previous studies found its regulation to myeloid immune cells, including macrophages. Aberrant infiltration and functions of macrophages are commonly found in oral squamous cell carcinoma (OSCC). In this study, we analyzed the effects of fucoidan on invasion of OSCC cells, and their regulation to macrophages, trying to evaluate its role as a potential therapy for OSCC. CAL27 and THP-1-derived macrophages were used as models for OSCC cells and tumor-infiltrated macrophages in the in vitro study, respectively. The effects of fucoidan on invasion of OSCC cells and their recruitment to macrophages were analyzed by transwell assay. KIF4A siRNA transfection was performed to investigate its role in fucoidan-modulated OSCC cells invasion. CCL3-neutralizing antibody was added into the conditioned medium of OSCC cells to evaluate its role in fucoidan-mediated macrophages recruitment and re-education. Fucoidan reduced the invasive potential of CAL27 cells with a decrease of MMP-2 and KIF4A transcription. KIF4A knockdown in CAL27 cells led to decreased invasion and MMP-2 expression. The conditioned medium of fucoidan-treated CAL27 cells promoted recruitment and inflammatory cytokines secretion on THP-1-derived macrophages. Further analysis found that fucoidan increased CCL3 production in CAL27 cells. Blocking CCL3 expression reversed the effects of fucoidan on macrophage recruitment and re-education. Our study found that fucoidan regulated the invasion of OSCC cells and also their recruiting and re-educating effects on macrophages, suggesting it could be a complementary approach in the treatment of OSCC.

Keywords: Fucoidan; Invasion; Macrophage; Oral squamous cell carcinoma; Recruitment.

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Carcinoma, Squamous Cell / drug therapy*
  • Carcinoma, Squamous Cell / immunology
  • Carcinoma, Squamous Cell / pathology
  • Cell Communication / drug effects*
  • Cell Communication / immunology
  • Cell Line
  • Cell Line, Tumor
  • Chemokine CCL3 / biosynthesis
  • Head and Neck Neoplasms / drug therapy*
  • Head and Neck Neoplasms / immunology
  • Head and Neck Neoplasms / pathology
  • Humans
  • Kinesins / biosynthesis
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / pathology
  • Matrix Metalloproteinase 2 / biosynthesis
  • Monocytes / cytology
  • Monocytes / drug effects
  • Neoplasm Invasiveness
  • Polysaccharides / pharmacology*
  • Squamous Cell Carcinoma of Head and Neck
  • Tongue Neoplasms / drug therapy*
  • Tongue Neoplasms / immunology
  • Tongue Neoplasms / pathology

Substances

  • Antineoplastic Agents
  • CCL3 protein, human
  • Chemokine CCL3
  • Polysaccharides
  • fucoidan
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
  • KIF4A protein, human
  • Kinesins