Lactic Acidosis Together with GM-CSF and M-CSF Induces Human Macrophages toward an Inflammatory Protumor Phenotype
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Paolini, Lea
Adam, Clement
Beauvillain, Celine
Preisser, Laurence
Blanchard, Simon
Pignon, Pascale
Seegers, Valerie
Chevalier, Louise-Marie
Campone, Mario
Wernert, Romuald
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American Association for Cancer Research
Abstract
In established tumors, tumor-associated macrophages (TAM)
orchestrate nonresolving cancer-related inflammation and produce
mediators favoring tumor growth, metastasis, and angiogenesis.
However, the factors conferring inflammatory and protumor properties on human macrophages remain largely unknown. Most solid
tumors have high lactate content. We therefore analyzed the impact
of lactate on human monocyte differentiation. We report that
prolonged lactic acidosis induces the differentiation of monocytes
into macrophages with a phenotype including protumor and
inflammatory characteristics. These cells produce tumor growth
factors, inflammatory cytokines, and chemokines as well as low
amounts of IL10. These effects of lactate require its metabolism and
are associated with hypoxia-inducible factor-1a stabilization. The
expression of some lactate-induced genes is dependent on autocrine
M-CSF consumption. Finally, TAMs with protumor and inflammatory characteristics (VEGFhigh CXCL8þ IL1bþ) are found in
solid ovarian tumors. These results show that tumor-derived lactate
links the protumor features of TAMs with their inflammatory
properties. Treatments that reduce tumor glycolysis or tumorassociated acidosis may help combat cancer.
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Cancer Immunology Research
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Restricted until
2037-12-31
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