Relationship between Fusobacterium nucleatum and antitumor immunity in colorectal cancer liver metastasis
DNA, Bacterial
Male
Fusobacterium nucleatum
Myeloid-Derived Suppressor Cells
Liver Neoplasms
Original Articles
CD8-Positive T-Lymphocytes
Middle Aged
3. Good health
03 medical and health sciences
0302 clinical medicine
Tumor-Associated Macrophages
Humans
Female
Lymphocyte Count
Colorectal Neoplasms
DOI:
10.1111/cas.15126
Publication Date:
2021-08-31T21:28:06Z
AUTHORS (17)
ABSTRACT
AbstractFusobacterium nucleatum has been detected in 8%‐13% of human colorectal cancer, and shown to inhibit immune responses against primary colorectal tumors in animal models. Thus, we hypothesized that the presence of F. nucleatum might be associated with reduced T cell density in colorectal cancer liver metastases (CRLM). We quantified F. nucleatum DNA in 181 CRLM specimens using quantitative PCR assay. The densities of CD8+ T cells, CD33+ cells (marker for myeloid‐derived suppressor cells [MDSCs]), and CD163+ cells (marker for tumor‐associated macrophages [TAMs]) in CRLM tissue were determined by immunohistochemical staining. Fusobacterium nucleatum was detected in eight (4.4%) of 181 CRLM specimens. Compared with F. nucleatum‐negative CRLM, F. nucleatum‐positive CRLM showed significantly lower density of CD8+ T cells (P = .033) and higher density of MDSCs (P = .001). The association of F. nucleatum with the density of TAMs was not statistically significant (P = .70). The presence of F. nucleatum is associated with a lower density of CD8+ T cells and a higher density of MDSCs in CRLM tissue. Upon validation, our findings could provide insights to develop strategies that involve targeting microbiota and immune cells for the prevention and treatment of CRLM.
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