Myeloid cells are a key determinant of tumor progression and patient outcomes in a range of cancers and are therefore being actively pursued as targets of new immunotherapies. The recent use of high-dimensional single-cell approaches, e.g., mass cytometry and single-cell RNA-sequencing (scRNA-seq) has reinforced the predominance of myeloid cells in the tumor microenvironment and uncovered their phenotypic diversity in different cancers. The cancerous metabolic environment has emerged as a critical modulator of myeloid cell functions in anti-tumor immunity versus immune suppression and immune evasion. Here, we discuss mechanisms of immune-metabolic crosstalk in tumorigenesis, with a particular focus on the tumor-associated myeloid cell's metabolic programs. We highlight the impact of several metabolic pathways on the pro-tumoral functions of tumor-associated macrophages and myeloid-derived suppressor cells and discuss the potential myeloid cell metabolic checkpoints for cancer immunotherapy, either as monotherapies or in combination with other immunotherapies.
机构:
Univ Med Ctr, Inst Translat Immunol, Mainz, Germany
Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02115 USAUniv Med Ctr, Dept Dermatol, Langenbeckstr 1, D-55131 Mainz, Germany
Schuppan, Detlef
Tuettenberg, Andrea
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Univ Med Ctr, Dept Dermatol, Langenbeckstr 1, D-55131 Mainz, GermanyUniv Med Ctr, Dept Dermatol, Langenbeckstr 1, D-55131 Mainz, Germany
机构:
Univ Calif San Diego, Moores UCSD Canc Ctr, 3855 Hlth Sci Dr, La Jolla, CA 92093 USAUniv Calif San Diego, Moores UCSD Canc Ctr, 3855 Hlth Sci Dr, La Jolla, CA 92093 USA
Schmid, Michael C.
Varner, Judith A.
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Univ Calif San Diego, Moores UCSD Canc Ctr, 3855 Hlth Sci Dr, La Jolla, CA 92093 USAUniv Calif San Diego, Moores UCSD Canc Ctr, 3855 Hlth Sci Dr, La Jolla, CA 92093 USA