NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE249702 Query DataSets for GSE249702
Status Public on May 01, 2024
Title NAB2-STAT6 drives an EGR1-dependent neuroendocrine program in Solitary Fibrous Tumors (RNA-Seq)
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary The pathogenesis of many rare tumor types is poorly understood, preventing the design of effective treatments. Solitary Fibrous Tumors (SFTs) are neoplasms of mesenchymal origin that affect 1/1,000,000 individuals every year and are clinically assimilated to sarcomas. SFTs are commonly found throughout the body and can be surgically removed upon diagnosis. However, 30-40% of tumors become aggressive and can locally relapse or metastasize. There are no effective treatments for malignant SFTs to date. The molecular hallmark of SFTs is a gene fusion between the NAB2 and STAT6 loci on chromosome 12, resulting in a chimeric protein of poorly characterized function called NAB2-STAT6. We use primary samples and an inducible cell model to discover that NAB2-STAT6 operates as a transcriptional coactivator for a specific set of enhancers and promoters that are normally targeted by the EGR1 transcription factor. In physiological conditions, NAB2 is primarily localized to the cytoplasm and only a small nuclear fraction is available to operate as a co-activator of EGR1 targets. NAB2-STAT6 redirects NAB1, NAB2, and additional EGR1 to the nucleus and bolster the expression of neuronal EGR1 targets. The STAT6 moiety of the fusion protein is a major driver of its nuclear localization and further contributes to NAB2’s co-activating abilities. In primary tumors, NAB2-STAT6 activates a neuroendocrine gene signature that sets it apart from most sarcomas. These discoveries provide new insight into the pathogenesis of SFTs and reveal new targets with therapeutic potential.
 
Overall design 3' - mRNA Seq was done in U2OS cells infected with doxycycline inducible NAB2-STAT6 expression plasmids without doxycycline treatment and after 1, 2, and 3 days of 1ug/mL doxycycline.
 
Contributor(s) Hill C, Gardini A
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Dec 08, 2023
Last update date May 01, 2024
Contact name Alessandro Gardini
E-mail(s) agardini@wistar.org
Phone 2158983755
Organization name The Wistar Institute
Lab Gardini Lab
Street address 3601 Spruce St, Room 230
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
Platforms (1)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (16)
GSM7959569 U2OS, pLVX-NAB2-STAT6, 1 day doxycycline, 3' mRNA-seq, biol rep1
GSM7959570 U2OS, pLVX-NAB2-STAT6, 1 day doxycycline, 3' mRNA-seq, biol rep2
GSM7959571 U2OS, pLVX-NAB2-STAT6, 1 day doxycycline, 3' mRNA-seq, biol rep3
This SubSeries is part of SuperSeries:
GSE249703 NAB2-STAT6 drives an EGR1-dependent neuroendocrine program in Solitary Fibrous Tumors
Relations
BioProject PRJNA1050217

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE249702_RAW.tar 200.9 Mb (http)(custom) TAR (of BW, TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap