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Status |
Public on Jul 27, 2021 |
Title |
FGFR1 associates with gene promoters and regulates gene transcription: Implications for endocrine resistance in ER+/FGFR1-amplified breast cancer (RNA-seq) |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Using ChIP-Seq analysis of ER+/FGFR1-amplified breast cancer cells and PDXs, we found FGFR1 occupancy at transcription start sites with high overlap with histone modifications associated with active gene transcription. Mass spectrometry analysis of the nuclear and chromatin-bound FGFR1 interactome identified RNA-Polymerase II (Pol II) and FOXA1, with FOXA1 silencing impairing FGFR1 recruitment to chromatin. Transduction of FGFR1(SP-)(NLS) into MCF7 cells resulted in overexpression of nuclear FGFR1 and resistance to antiestrogens. Finally, an expression signature associated with nuclear FGFR1 correlated with endocrine resistance in patients treated with antiestrogens
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Overall design |
Examination of transcriptome of ER+/FGFR1-amplified human breast cancer CAMA1 cells. Three biological replicates
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Contributor(s) |
Servetto A, Kollipara RK, Kittler R, Arteaga C |
Citation(s) |
34011560 |
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Submission date |
Apr 08, 2020 |
Last update date |
Jul 27, 2021 |
Contact name |
Ralf Kittler |
E-mail(s) |
Ralf.Kittler@UTSouthwestern.edu
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Organization name |
University of Texas Southwestern Medical Center
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Street address |
5323 Harry Hines Blvd
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City |
Dallas |
State/province |
Texas |
ZIP/Postal code |
75390 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (3) |
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This SubSeries is part of SuperSeries: |
GSE148313 |
FGFR1 associates with gene promoters and regulates gene transcription: Implications for endocrine resistance in ER+/FGFR1-amplified breast cancer |
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Relations |
BioProject |
PRJNA623904 |
SRA |
SRP255745 |