TY - JOUR
T1 - Tumor targeting by Fusobacterium nucleatum
T2 - A Pilot Study and future Perspectives
AU - Abed, Jawad
AU - Maalouf, Naseem
AU - Parhi, Lishay
AU - Chaushu, Stella
AU - Mandelboim, Ofer
AU - Bachrach, Gilad
N1 - Publisher Copyright:
© 2017 Abed, Maalouf, Parhi, Chaushu, Mandelboim and Bachrach.
PY - 2017/6/30
Y1 - 2017/6/30
N2 - 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.
AB - 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.
KW - Adenocarcinoma
KW - Bacterioncology
KW - Cancer
KW - Fusobacterium nucleatum
KW - Gal-GalNAc
UR - http://www.scopus.com/inward/record.url?scp=85027498147&partnerID=8YFLogxK
U2 - 10.3389/fcimb.2017.00295
DO - 10.3389/fcimb.2017.00295
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C2 - 28713780
AN - SCOPUS:85027498147
SN - 2235-2988
VL - 7
JO - Frontiers in Cellular and Infection Microbiology
JF - Frontiers in Cellular and Infection Microbiology
IS - JUN
M1 - 295
ER -