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M2‐TAM‐derived exosomal NEAT1 promoted HCC tumor growth in vivo. C57BL/6 mice were injected with HCC cells (5 × 106 cells per mouse) and treated with M2‐exo, M2‐exo‐shNEAT1, or saline every 3 days. (A‐C) The size and volume of tumors were presented. (D) CD8 level in tumor tissues was assessed by immunohistochemistry. The measurement data were presented as mean ± SD. n = 5. ***p < 0.001.
