{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["12(6)"],"submitter":["Bell JL"],"pubmed_abstract":["Neuroblastoma is the most common solid tumor in childhood and represents 15% of all children's cancer deaths. We have previously demonstrated that tripartite motif 16 (TRIM16), a member of the RING B-box coiled-coil (RBCC)/tripartite totif (TRIM) protein family, has significant effects on neuroblastoma proliferation and migration in vitro and tumorigenicity in vivo. However, the mechanism by which this putative tumor suppressor influences cell proliferation and tumorigenicity was undetermined. Here we show, for the first time, TRIM16's striking pattern of expression and dynamic localization during cell cycle progression and neuroblastoma tumor development. In a tyrosine hydroxylase MYCN (TH-MYCN) neuroblastoma mouse model, immunohistochemical staining revealed strong nuclear TRIM16 express"],"journal":["Cell cycle (Georgetown, Tex.)"],"pagination":["889-98"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3637347"],"repository":["biostudies-literature"],"pubmed_title":["TRIM16 inhibits neuroblastoma cell proliferation through cell cycle regulation and dynamic nuclear localization."],"pmcid":["PMC3637347"],"pubmed_authors":["Kavallaris M","Bell JL","Marshall GM","Malyukova A","Cheung BB"],"additional_accession":[]},"is_claimable":false,"name":"TRIM16 inhibits neuroblastoma cell proliferation through cell cycle regulation and dynamic nuclear localization.","description":"Neuroblastoma is the most common solid tumor in childhood and represents 15% of all children's cancer deaths. We have previously demonstrated that tripartite motif 16 (TRIM16), a member of the RING B-box coiled-coil (RBCC)/tripartite totif (TRIM) protein family, has significant effects on neuroblastoma proliferation and migration in vitro and tumorigenicity in vivo. However, the mechanism by which this putative tumor suppressor influences cell proliferation and tumorigenicity was undetermined. Here we show, for the first time, TRIM16's striking pattern of expression and dynamic localization during cell cycle progression and neuroblastoma tumor development. In a tyrosine hydroxylase MYCN (TH-MYCN) neuroblastoma mouse model, immunohistochemical staining revealed strong nuclear TRIM16 express","dates":{"release":"2013-01-01T00:00:00Z","publication":"2013 Mar","modification":"2026-05-07T02:39:11.251Z","creation":"2026-04-07T22:32:05.431Z"},"accession":"S-EPMC3637347","cross_references":{"pubmed":["23422002"],"doi":["10.4161/cc.23825"]}}