Periodontal pathogens promote epithelial-mesenchymal transition in oral squamous carcinoma cells in vitro

Cell Adh Migr. 2018 Mar 4;12(2):127-137. doi: 10.1080/19336918.2017.1322253. Epub 2017 Sep 12.

Abstract

Epithelial-mesenchymal transition (EMT) is potentially involved in increasing metastasis of oral squamous cell carcinoma (OSCC). Periodontal pathogens are well-known for their ability to induce intense immune responses and here we investigated whether they are involved in inducing EMT. Cultures of OSCC cell line (H400) were treated separately with heat-killed periodontal pathogens F. nucleatum, or P. gingivalis or E. coli LPS for 8 d. EMT-associated features were assayed using sq-PCR and PCR-arrays, for EMT-related markers, and ELISAs for TGF-β1, TNF-α, and EGF. The migratory ability of cells was investigated using scratch and transwell migration assays. E-cadherin and vimentin expression was assessed using immunofluorescence while Snail activation was detected with immunocytochemistry. In addition, the integrity of the cultured epithelial layer was investigated using transepithelial electrical resistance (TEER). PCR data showed significant upregulation after 1, 5, and 8 d in transcription of mesenchymal markers and downregulation of epithelial ones compared with unstimulated controls, which were confirmed by immunofluorescence. Periodontal pathogens also caused a significant increase in level of all cytokines investigated which could be involved in EMT-induction and Snail activation. Exposure of cells to the bacteria increased migration and the rate of wound closure. Downregulation of epithelial markers also resulted in a significant decrease in impedance resistance of cell monolayers to passage of electrical current. These results suggested that EMT was likely induced in OSCC cells in response to stimulation by periodontal pathogens.

Keywords: cadherins; cytokines; invasiveness; mesenchymal cells; migration; neoplasm metastasis; oral keratinocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cadherins / metabolism
  • Carcinoma, Squamous Cell / microbiology*
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Epithelial Cells / microbiology
  • Epithelial Cells / pathology*
  • Epithelial-Mesenchymal Transition / physiology*
  • Escherichia coli / pathogenicity*
  • Humans
  • Snail Family Transcription Factors / metabolism
  • Transcription Factors / metabolism
  • Vimentin / metabolism

Substances

  • Cadherins
  • Snail Family Transcription Factors
  • Transcription Factors
  • Vimentin