NAB2-STAT6 fusion protein mediates cell proliferation and oncogenic progression via EGR-1 regulation

Solitary fibrous tumors are rare mesenchymal tumors derived from soft tissues and vascular walls. NAB2-STAT6 fusion gene serves as a marker gene for this disease and consists of the truncated repressor domain of NGFI-A-Binding protein 2 (NAB2) and the intact activation domain of STAT6. In this study...

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Veröffentlicht in:Biochemical and biophysical research communications 2020-05, Vol.526 (2), p.287-292
Hauptverfasser: Park, Ye-Seul, Kim, Hyeng-Soo, Kim, Ju-Heon, Choi, Sung-Hun, Kim, Da-Som, Ryoo, Zae Young, Kim, Jae-Young, Lee, Sanggyu
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Sprache:eng
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Zusammenfassung:Solitary fibrous tumors are rare mesenchymal tumors derived from soft tissues and vascular walls. NAB2-STAT6 fusion gene serves as a marker gene for this disease and consists of the truncated repressor domain of NGFI-A-Binding protein 2 (NAB2) and the intact activation domain of STAT6. In this study, we found that EGR-1 and the proliferation-related EGR-1 target gene IGF2 were upregulated in NIH-3T3 cells transfected with NAB2-STAT6. Additionally, p-Rb (Ser795) and cyclin D1 levels were upregulated, and cell proliferation was also enhanced. We identified that treatment with the IGF2 inhibitor reduced cell proliferation in NIH-3T3 cells transfected with NAB2-STAT6. The oncogenic progression was enhanced in NIH-3T3 cells transfected with NAB2-STAT6 compared with those transfected with the empty vector. Taken together, our study suggests that the NAB2-STAT6 fusion gene is associated with cell proliferation through EGR-1 transcriptional expression and IGF2 can be a drug target for the treatment of solitary fibrous tumors. •NAB2-STAT6 fusion enhances cell proliferation and migration.•The NAB2-STAT6 fusion protein affects the EGR-1 target gene IGF2 in NIH-3T3 cells.•IGF2 inhibitors suppress the proliferation and migration of NIH-3T3 cells with NAB2-STAT6.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2020.03.090