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Status |
Public on Aug 23, 2017 |
Title |
Targeting the androgen receptor N-terminus via the cochaperone Bag-1L [RNA-seq C-terminal mutant] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Targeting the activation function-1 (AF-1) at the N-terminus of the androgen receptor (AR) is an attractive therapeutic alternative to the current approaches to inhibit AR action in prostate cancer (PCa). Here we show that the AR AF-1 is bound by the BAG domain of the cochaperone Bag-1L. Mutations in this domain or loss of Bag-1L abrogates AR signaling and reduces PCa growth. Correspondingly, Bag-1L protein levels increase with progression of primary prostate tumors to castration-resistant PCa, correlating inversely with patient response to abiraterone therapy. Intriguingly, BAG domain residues important for its interaction with the AR AF-1 overlap a potentially druggable pocket of this protein. Bag-1L is therefore a putative therapeutic target for the inhibition of AR AF-1 activity.
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Overall design |
We performed transcriptome analysis (RNA-Seq) of 2 cell lines (LNCaP Bag-1L WT and LNCaP Bag-1L CMut) cultured under hormone-starvation conditions for 72 h and then treated with vehicle (ethanol, EtOH) or 10 nM Dihydrotestosterone (DHT) for 16 h. Biological duplicate samples were analyzed for each cell line and each treatment condition.
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Contributor(s) |
Cato L, Neeb A, Armant O, Gourain V, Cato AC, Brown M |
Citation(s) |
28826504, 35479411 |
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Submission date |
Aug 02, 2017 |
Last update date |
May 05, 2022 |
Contact name |
Laura Cato |
E-mail(s) |
laura_cato@dfci.harvard.edu
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Organization name |
Dana-Farber Cancer Institute
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Department |
Medical Oncology
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Street address |
450 Brookline Ave., D728
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
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Platforms (1) |
GPL18460 |
Illumina HiSeq 1500 (Homo sapiens) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE89939 |
Targeting the androgen receptor N-terminus via the cochaperone Bag-1L |
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Relations |
BioProject |
PRJNA396941 |
SRA |
SRP114702 |