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Illustration of the conclusions: miR‐3184‐3p promoted glioma progression in two ways. On the one hand, miR‐3184 enhanced glioma tumorigenesis via targeting PDCD4. On the other hand, miR‐3184 was enriched in glioma‐derived exosomes and induced M2‐like polarization in macrophages, which in return aggravated the glioma malignancy
