Abstract
The majority of tumor-associated macrophages exhibit the M2 phenotype, which is an important determinant of tumor development and metastasis. Reducing the number of intratumoral M2 macrophages is an urgent task. It has been revealed that blockade of glycolysis by sodium oxamate or the glutamine-free medium both suppresses the ability of high-metastatic (LLC) and low-metastatic (LLCR9) Lewis lung carcinoma cells to macrophage reprogramming into the M2 phenotype.
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