| Literature DB >> 27346356 |
Xu Li1, Wenqi Wang1, Yuanxin Xi2, Min Gao1, MyKim Tran1, Kathryn E Aziz1, Jun Qin3, Wei Li2, Junjie Chen4.
Abstract
By combining the results of a large-scale proteomic analysis of the human transcription factor interaction network with knowledge databases, we identified FOXR2 as one of the top-ranked candidate proto-oncogenes. Here, we show that FOXR2 forms a stable complex with MYC and MAX and subsequently regulates cell proliferation by promoting MYC's transcriptional activities. We demonstrate that FOXR2 is highly expressed in several breast, lung, and liver cancer cell lines and related patient tumor samples, while reduction of FOXR2 expression in a xenograft model inhibits tumor growth. These results indicate that FOXR2 acts with MYC to promote cancer cell proliferation, which is a potential tumor-specific target for therapeutic intervention against MYC-driven cancers.Entities:
Keywords: FOXR2; MYC; forkhead box; protein-protein interaction
Mesh:
Substances:
Year: 2016 PMID: 27346356 PMCID: PMC4946253 DOI: 10.1016/j.celrep.2016.06.004
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423