
Recent studies revealed that vasculogenic mimicry (VM) had been considered a potential factor for the failure of antiangiogenic therapy in patients with tumors. Thus, inhibition of VM formation might be a potential target for improving the outcome of antiangiogenic strategies. The study found that the combined treatment of anti‐L1CAM neutralizing monoclonal antibody and bevacizumab increases efficacy beyond that of bevacizumab alone and suppresses glioma growth in vivo, indicating that the inhibition of L1CAM‐mediated VM formation might efficiently improve the effect of antiangiogenic treatment for glioma patients. Together, the findings demonstrated a critical role of L1CAM in regulating VM formation in glioma and that L1CAM might be a potential target for ameliorating tumor resistance to antiangiogenic therapy in glioma patients.
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