Fibroblast growth factor receptor 3 interacts with and activates TGFβ-activated kinase 1 tyrosine phosphorylation and NFκB signaling in multiple myeloma and bladder cancer
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
P30 CA062203
NCI NIH HHS - United States
PubMed
24466111
PubMed Central
PMC3900522
DOI
10.1371/journal.pone.0086470
PII: PONE-D-13-33878
Knihovny.cz E-zdroje
- MeSH
- apoptóza MeSH
- buněčná adheze MeSH
- fosforylace MeSH
- imunoprecipitace MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- lidé MeSH
- MAP kinasy kinas (kinas) genetika metabolismus MeSH
- messenger RNA genetika MeSH
- mnohočetný myelom genetika metabolismus patologie MeSH
- nádorové biomarkery genetika metabolismus MeSH
- nádorové buňky kultivované MeSH
- nádory močového měchýře genetika metabolismus patologie MeSH
- NF-kappa B genetika metabolismus MeSH
- peptidové fragmenty MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- proliferace buněk MeSH
- receptor fibroblastových růstových faktorů, typ 3 genetika metabolismus MeSH
- sekvenční analýza hybridizací s uspořádaným souborem oligonukleotidů MeSH
- signální transdukce MeSH
- spektrometrie hmotnostní - ionizace laserem za účasti matrice MeSH
- stanovení celkové genové exprese MeSH
- techniky dvojhybridového systému MeSH
- transformující růstový faktor beta genetika metabolismus MeSH
- tyrosin metabolismus MeSH
- western blotting MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- FGFR3 protein, human MeSH Prohlížeč
- MAP kinase kinase kinase 7 MeSH Prohlížeč
- MAP kinasy kinas (kinas) MeSH
- messenger RNA MeSH
- nádorové biomarkery MeSH
- NF-kappa B MeSH
- peptidové fragmenty MeSH
- receptor fibroblastových růstových faktorů, typ 3 MeSH
- transformující růstový faktor beta MeSH
- tyrosin MeSH
Cancer is a major public health problem worldwide. In the United States alone, 1 in 4 deaths is due to cancer and for 2013 a total of 1,660,290 new cancer cases and 580,350 cancer-related deaths are projected. Comprehensive profiling of multiple cancer genomes has revealed a highly complex genetic landscape in which a large number of altered genes, varying from tumor to tumor, impact core biological pathways and processes. This has implications for therapeutic targeting of signaling networks in the development of treatments for specific cancers. The NFκB transcription factor is constitutively active in a number of hematologic and solid tumors, and many signaling pathways implicated in cancer are likely connected to NFκB activation. A critical mediator of NFκB activity is TGFβ-activated kinase 1 (TAK1). Here, we identify TAK1 as a novel interacting protein and target of fibroblast growth factor receptor 3 (FGFR3) tyrosine kinase activity. We further demonstrate that activating mutations in FGFR3 associated with both multiple myeloma and bladder cancer can modulate expression of genes that regulate NFκB signaling, and promote both NFκB transcriptional activity and cell adhesion in a manner dependent on TAK1 expression in both cancer cell types. Our findings suggest TAK1 as a potential therapeutic target for FGFR3-associated cancers, and other malignancies in which TAK1 contributes to constitutive NFκB activation.
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