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

Ye Seul Park, Hyeng Soo Kim, Ju Heon Kim, Sung Hun Choi, Da Som Kim, Zae Young Ryoo, Jae Young Kim, Sanggyu Lee

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)287-292
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume526
Issue number2
DOIs
StatePublished - 28 May 2020

Keywords

  • Chromeceptin
  • EGR-1
  • IGF2
  • NAB2-STAT6
  • Solitary fibrous tumor

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