Next tumor cell migration relies on the regulation of various biological processes, including actin cytoskeleton dynamics, integrin‐dependent adhesion and proteolytic cleavage of ECM proteins.[29] To gain deeper insights into the mechanism of action through which LIN28B sustains tumor cell dissemination, we employed a genetically modified doxycycline‐inducible cell system to achieve ectopically overexpressed LIN28B oncogene in the SH‐SY5Y neuroblastoma cells. This evidence concerns the gene LIN28B and neuroblastoma.