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.
| Original language | English |
|---|---|
| Article number | 295 |
| Journal | Frontiers in Cellular and Infection Microbiology |
| Volume | 7 |
| Issue number | JUN |
| DOIs | |
| State | Published - 30 Jun 2017 |
Bibliographical note
Publisher Copyright:© 2017 Abed, Maalouf, Parhi, Chaushu, Mandelboim and Bachrach.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adenocarcinoma
- Bacterioncology
- Cancer
- Fusobacterium nucleatum
- Gal-GalNAc
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