Considering the crosstalk between metabolic dysregulation and immune cell infiltration, we detected and validated PD‐L1 expression in the different groups by immunohistochemistry, and the results showed an increasing trend of PD‐L1 expression within the TME in the U14‐oeFOXP1 group (Figure 8n ).
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NAT10/ac4C/FOXP1 Promotes Malignant Progression and Facilitates Immunosuppression by Reprogramming Glycolytic Metabolism in Cervical Cancer.
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