Treponema denticola chymotrypsin-like proteinase may contribute to orodigestive carcinogenesis through immunomodulation

Br J Cancer. 2018 Feb 6;118(3):428-434. doi: 10.1038/bjc.2017.409. Epub 2017 Nov 16.

Abstract

Background: Periodontal pathogens have been linked to oral and gastrointestinal (orodigestive) carcinogenesis. However, the exact mechanisms remain unknown. Treponema denticola (Td) is associated with severe periodontitis, a chronic inflammatory disease leading to tooth loss. The anaerobic spirochete Td is an invasive bacteria due to its major virulence factor chymotrypsin-like proteinase. Here we aimed to investigate the presence of Td chymotrypsin-like proteinase (Td-CTLP) in major orodigestive tumours and to elucidate potential mechanisms for Td to contribute to carcinogenesis.

Methods: The presence of Td-CTLP within orodigestive tumour tissues was examined using immunohistochemistry. Oral, tonsillar, and oesophageal squamous cell carcinomas, alongside gastric, pancreatic, and colon adenocarcinomas were stained with a Td-CTLP-specific antibody. Gingival tissue from periodontitis patients served as positive controls. SDS-PAGE and immunoblot were used to analyse the immumodulatory activity of Td-CTLP in vitro.

Results: Td-CTLP was present in majority of orodigestive tumour samples. Td-CTLP was found to convert pro MMP-8 and -9 into their active forms. In addition, Td-CTLP was able to degrade the proteinase inhibitors TIMP-1, TIMP-2, and α-1-antichymotrypsin, as well as complement C1q.

Conclusions: Because of its presence within tumours and regulatory activity on proteins critical for the regulation of tumour microenvironment and inflammation, the Td-CTLP may contribute to orodigestive carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / chemistry*
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Carcinoma, Squamous Cell / chemistry*
  • Carcinoma, Squamous Cell / metabolism
  • Carcinoma, Squamous Cell / pathology
  • Cell Transformation, Neoplastic / immunology*
  • Chymases / analysis*
  • Colonic Neoplasms / chemistry
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology
  • Complement C1q / metabolism
  • Digestive System Neoplasms / chemistry*
  • Digestive System Neoplasms / metabolism
  • Digestive System Neoplasms / pathology
  • Esophageal Neoplasms / chemistry
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology
  • Head and Neck Neoplasms / chemistry*
  • Head and Neck Neoplasms / metabolism
  • Head and Neck Neoplasms / pathology
  • Humans
  • Matrix Metalloproteinase 8 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Mouth Neoplasms / chemistry
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / pathology
  • Pancreatic Neoplasms / chemistry
  • Pancreatic Neoplasms / metabolism
  • Pancreatic Neoplasms / pathology
  • Stomach Neoplasms / chemistry
  • Stomach Neoplasms / pathology
  • Tissue Inhibitor of Metalloproteinase-1 / metabolism
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism
  • Tonsillar Neoplasms / chemistry
  • Tonsillar Neoplasms / metabolism
  • Tonsillar Neoplasms / pathology
  • Treponema denticola / enzymology*
  • alpha 1-Antichymotrypsin / metabolism

Substances

  • TIMP1 protein, human
  • TIMP2 protein, human
  • Tissue Inhibitor of Metalloproteinase-1
  • alpha 1-Antichymotrypsin
  • Tissue Inhibitor of Metalloproteinase-2
  • Complement C1q
  • Chymases
  • Matrix Metalloproteinase 8
  • Matrix Metalloproteinase 9