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

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作者
Lishay Parhi
Tamar Alon-Maimon
Asaf Sol
Deborah Nejman
Amjad Shhadeh
Tanya Fainsod-Levi
Olga Yajuk
Batya Isaacson
Jawad Abed
Naseem Maalouf
Aviram Nissan
Judith Sandbank
Einav Yehuda-Shnaidman
Falk Ponath
Jörg Vogel
Ofer Mandelboim
Zvi Granot
Ravid Straussman
Gilad Bachrach
机构
[1] The Hebrew University-Hadassah School of Dental Medicine,The Institute of Dental Sciences
[2] Weizmann Institute of Science,Department of Molecular Cell Biology
[3] Hebrew University-Hadassah Medical School,Department of Developmental Biology and Cancer Research, Institute for Medical Research Israel Canada (IMRIC)
[4] Hebrew University-Hadassah Medical School,Department of Immunology and Cancer Research, Institute for Medical Research Israel Canada (IMRIC)
[5] The Chaim Sheba Medical Center,Department of General and Oncological Surgery
[6] Tel Hashomer,Surgery C
[7] The Pathology Institute,Institute for Molecular Infection Biology, Medical Faculty
[8] Maccabi Healthcare Services,undefined
[9] Helmholtz Institute for RNA-based Infection Research (HIRI),undefined
[10] Helmholtz Center for Infection Research (HZI),undefined
[11] University of Würzburg,undefined
来源
Nature Communications | / 11卷
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摘要
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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