Breast cancer colonization by Fusobacterium nucleatum accelerates tumor growth and metastatic progression

Lishay Parhi(Hebrew University of Jerusalem), Tamar Alon‐Maimon(Hebrew University of Jerusalem), Asaf Sol(Hebrew University of Jerusalem), Deborah Nejman(Weizmann Institute of Science), Amjad Shhadeh(Hebrew University of Jerusalem), Tanya Fainsod-Levi, Olga Yajuk, Batya Isaacson, Jawad Abed(Hebrew University of Jerusalem), Naseem Maalouf(Hebrew University of Jerusalem), Aviram Nissan(Sheba Medical Center), Judith Sandbank(Maccabi Institute for Health Services Research), Einav Yehuda‐Shnaidman(Maccabi Institute for Health Services Research), Falk Ponath(Helmholtz Institute for RNA-based Infection Research), Jörg Vogel(University of Würzburg), Ofer Mandelboim, Zvi Granot, Ravid Straussman(Weizmann Institute of Science), Gilad Bachrach(Hebrew University of Jerusalem)
Nature Communications
June 26, 2020
Cited by 698Open Access
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Abstract

Fusobacterium nucleatum is an oral anaerobe recently found to be prevalent in human colorectal cancer (CRC) where it is associated with poor treatment outcome. In mice, hematogenous F. nucleatum can colonize CRC tissue using its lectin Fap2, which attaches to tumor-displayed Gal-GalNAc. Here, we show that Gal-GalNAc levels increase as human breast cancer progresses, and that occurrence of F. nucleatum gDNA in breast cancer samples correlates with high Gal-GalNAc levels. We demonstrate Fap2-dependent binding of the bacterium to breast cancer samples, which is inhibited by GalNAc. Intravascularly inoculated Fap2-expressing F. nucleatum ATCC 23726 specifically colonize mice mammary tumors, whereas Fap2-deficient bacteria are impaired in tumor colonization. Inoculation with F. nucleatum suppresses accumulation of tumor infiltrating T cells and promotes tumor growth and metastatic progression, the latter two of which can be counteracted by antibiotic treatment. Thus, targeting F. nucleatum or Fap2 might be beneficial during treatment of breast cancer.


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