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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
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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.
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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.
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Contributor(s) |
Hill C, Gardini A |
Citation missing |
Has this study been published? Please login to update or notify GEO. |
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Submission date |
Dec 08, 2023 |
Last update date |
May 01, 2024 |
Contact name |
Alessandro Gardini |
E-mail(s) |
agardini@wistar.org
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Phone |
2158983755
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Organization name |
The Wistar Institute
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Lab |
Gardini Lab
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Street address |
3601 Spruce St, Room 230
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City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
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Platforms (1) |
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Samples (16)
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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 |
GSM7959572 |
U2OS, pLVX-NAB2-STAT6, 1 day doxycycline, 3' mRNA-seq, biol rep4 |
GSM7959573 |
U2OS, pLVX-NAB2-STAT6, 2 days doxycycline, 3' mRNA-seq, biol rep1 |
GSM7959574 |
U2OS, pLVX-NAB2-STAT6, 2 days doxycycline, 3' mRNA-seq, biol rep2 |
GSM7959575 |
U2OS, pLVX-NAB2-STAT6, 2 days doxycycline, 3' mRNA-seq, biol rep3 |
GSM7959576 |
U2OS, pLVX-NAB2-STAT6, 2 days doxycycline, 3' mRNA-seq, biol rep4 |
GSM7959577 |
U2OS, pLVX-NAB2-STAT6, 3 days doxycycline, 3' mRNA-seq, biol rep1 |
GSM7959578 |
U2OS, pLVX-NAB2-STAT6, 3 days doxycycline, 3' mRNA-seq, biol rep2 |
GSM7959580 |
U2OS, pLVX-NAB2-STAT6, 3 days doxycycline, 3' mRNA-seq, biol rep3 |
GSM7959581 |
U2OS, pLVX-NAB2-STAT6, 3 days doxycycline, 3' mRNA-seq, biol rep4 |
GSM7959582 |
U2OS, pLVX-NAB2-STAT6, control, 3' mRNA-seq, biol rep1 |
GSM7959583 |
U2OS, pLVX-NAB2-STAT6, control, 3' mRNA-seq, biol rep2 |
GSM7959584 |
U2OS, pLVX-NAB2-STAT6, control, 3' mRNA-seq, biol rep3 |
GSM7959585 |
U2OS, pLVX-NAB2-STAT6, control, 3' mRNA-seq, biol rep4 |
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This SubSeries is part of SuperSeries: |
GSE249703 |
NAB2-STAT6 drives an EGR1-dependent neuroendocrine program in Solitary Fibrous Tumors |
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Relations |
BioProject |
PRJNA1050217 |
Supplementary file |
Size |
Download |
File type/resource |
GSE249702_RAW.tar |
200.9 Mb |
(http)(custom) |
TAR (of BW, TXT) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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