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Tumor Targeting by Fusobacterium nucleatum : A Pilot Study and Future Perspectives.
- Source :
-
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2017 Jun 30; Vol. 7, pp. 295. Date of Electronic Publication: 2017 Jun 30 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- Colorectal adenocarcinoma (CRC) is a common tumor with high mortality rates. Interestingly, CRC was found to be colonized by the oral anaerobic bacteria Fusobacterium nucleatum , which accelerates tumor progression and enables immune evasion. The CRC-specific colonization by fusobacteria is mediated through the recognition of tumor displayed Gal-GalNAc moieties by the fusobacterial Fap2 Gal-GalNAc lectin. Here, we show high Gal-GalNAc levels in additional adenocarcinomas including those found in the stomach, prostate, ovary, colon, uterus, pancreas, breast, lung, and esophagus. This observation coincides with recent reports that found fusobacterial DNA in some of these tumors. Given the tumorigenic role of fusobacteria and its immune evasion properties, we suggest that fusobacterial elimination might improve treatment outcome of the above tumors. Furthermore, as fusobacteria appears to specifically home-in to Gal-GalNAc-displaying tumors, it might be engineered as a platform for treating CRC and the above common, lethal, adenocarcinomas.
- Subjects :
- Adenocarcinoma pathology
Antigens, Tumor-Associated, Carbohydrate analysis
Colonic Neoplasms pathology
Fusobacterium nucleatum genetics
Fusobacterium nucleatum immunology
Host-Pathogen Interactions
Humans
Immune Evasion
Lectins metabolism
Liver Neoplasms pathology
Pilot Projects
Sarcoma pathology
Adenocarcinoma microbiology
Carcinogenesis pathology
Colonic Neoplasms microbiology
Fusobacterium nucleatum pathogenicity
Subjects
Details
- Language :
- English
- ISSN :
- 2235-2988
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- Frontiers in cellular and infection microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 28713780
- Full Text :
- https://doi.org/10.3389/fcimb.2017.00295