NFKB1 and neuroblastoma: DRR1, F-actin and COMMD1 form a complex in the nucleus, and the stability of COMMD1 in the complex is enhanced to promote the degradation of Nf-κB; DRR1 and COMMD1 inhibit cyclinD1 expression, G1/S transition and cell proliferation in neuroblastoma (79).