Proinflammatory and Cancer-Promoting Pathobiont Fusobacterium nucleatum Directly Targets Colorectal Cancer Stem Cells

Biomolecules. 2022 Sep 7;12(9):1256. doi: 10.3390/biom12091256.

Abstract

Intestinal bacterial communities participate in gut homeostasis and are recognized as crucial in bowel inflammation and colorectal cancer (CRC). Fusobacterium nucleatum (Fn), a pathobiont of the oral microflora, has recently emerged as a CRC-associated microbe linked to disease progression, metastasis, and a poor clinical outcome; however, the primary cellular and/or microenvironmental targets of this agent remain elusive. We report here that Fn directly targets putative colorectal cancer stem cells (CR-CSCs), a tumor cell subset endowed with cancer re-initiating capacity after surgery and chemotherapy. A patient-derived CSC line, highly enriched (70%) for the stem marker CD133, was expanded as tumor spheroids, dissociated, and exposed in vitro to varying amounts (range 100-500 MOI) of Fn. We found that Fn stably adheres to CSCs, likely by multiple interactions involving the tumor-associated Gal-GalNac disaccharide and the Fn-docking protein CEA-family cell adhesion molecule 1 (CEACAM-1), robustly expressed on CSCs. Importantly, Fn elicited innate immune responses in CSCs and triggered a growth factor-like, protein tyrosine phosphorylation cascade largely dependent on CEACAM-1 and culminating in the activation of p42/44 MAP kinase. Thus, the direct stimulation of CSCs by Fn may contribute to microbiota-driven colorectal carcinogenesis and represent a target for innovative therapies.

Keywords: PTPase; bacterial adhesins; cancer stem cells; carcino-embryonic antigen cell adhesion molecule-1; colorectal cancer; fusobacterium nucleatum; microbiota; tumor microenvironment; tumor spheroids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD
  • Cell Adhesion Molecules
  • Colorectal Neoplasms* / pathology
  • Disaccharides
  • Fusobacterium Infections* / complications
  • Fusobacterium Infections* / microbiology
  • Fusobacterium nucleatum / physiology
  • Humans
  • Neoplastic Stem Cells* / metabolism
  • Tyrosine

Substances

  • Antigens, CD
  • CD66 antigens
  • Cell Adhesion Molecules
  • Disaccharides
  • Tyrosine

Grants and funding

This research was funded by the Italian Ministry of Health, GR-2016-02364891 (to F.S. and M.F.) and Universita’ Cattolica del Sacro Cuore, intramural grant D.1-2020 (to G.B.P.).