| Literature DB >> 29501729 |
Hadjer Miloudi1, Karen Leroy2, Fabrice Jardin3, Brigitte Sola4.
Abstract
Primary mediastinal B-cell lymphoma (PMBL) is a distinct B-cell lymphoma subtype with unique clinicopathological and molecular features. PMBL cells are characterised by several genetic abnormalities that conduct to the constitutive activation of the Janus kinase 2/signal transducer and activator of transcription 6 (JAK2/STAT6) signalling pathway. Among recurrent genetic changes in PMBL, we previously reported that the XPO1 gene encoding exportin 1 that controls the nuclear export of cargo proteins and RNAs, is mutated (p.E571K) in about 25% of PMBL cases. We therefore hypothesized that STAT6 could be a cargo of XPO1 and that STAT6 cytoplasm/nucleus shuttle could be altered in a subset of PMBL cells. Using immunocytochemistry techniques as well as the proximity ligation assay, we showed that STAT6 bound XPO1 in PBML cell lines and in HEK-293 cells genetically engineered to produce STAT6. Moreover, XPO1-mediated export of STAT6 occurs in cells expressing either a wild-type or the E571K mutated XPO1 protein.Entities:
Keywords: B lymphoma; CRM1; PLA technology; SINE; STAT; XPO1 mutation
Mesh:
Substances:
Year: 2018 PMID: 29501729 DOI: 10.1016/j.cellsig.2018.02.016
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315