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| Status |
Public on Sep 22, 2022 |
| Title |
Targeted Escalation of Tyrosine Kinase Super-Enhancer Network Engineered by Acetylated HOXB13 Spurs Prostate Tumor Autonomy |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
While tissue and lineage-specific super-enhancers (SEs) regulate cell fate decision during development, the nature of Castration Resistant Prostate Cancer (CRPC)-specific SEs (CSEs) is unknown. Herein we report the lysine 13 (K13) acetylation of HOXB13 mediated by the histone acetyltransferase CBP/p300 regulates prostate tumor autonomy. The acK13-HOXB13 shadows H3K27ac at lineage specific SEs and surpasses it at CSEs. In contrast, mutation of HOXB13 at K13 sensitizes CRPCs to Enzalutamide, disables spheroid and xenograft tumor formation. Mechanistically, the acK13-HOXB13 interacts with chromatin remodeling bromodomain proteins to regulate tumor-specific CSE selection. These CSEs sprout at critical lineage genes NKX3-1, Androgen receptor (AR), AR regulator ACK1 tyrosine kinase and tyrosine kinase ligands regulating angiogenesis. Single-cell transcriptomic analysis of human prostate tumor organoids reveal ACK1 expression underlies sensitivity to the small molecule inhibitor (R)-9b over AR-targeted agents. Collectively, our studies reveal acK13-HOXB13 regulated epigenome as a key cog in prostate cancer cell autonomy.
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| Overall design |
Human prostate organoids were grown as described above. Single cell suspension was processed for library preparation as described in the 10X Genomics single cell suspension protocol. All samples were quantitated twice on the bioanalyzer and checked to ensure integrity. 10x Single Cell/Nuclei RNAseq Library and Sequencing Targeting 25K read pairs/cell. The samples amplified well for adequate libraries set up as per the 10X Genomics protocol. 25k depth per cell sequencing was performed using the NovaSeq S4. The Cell Ranger software was used to align the reads to the reference genome. Cloupe browser analysis was performed to generate the t-SNE plot and UMAP clustering analysis.
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| Contributor(s) |
Mahajan K, Cliften P |
| Citation(s) |
35849143 |
| Submission date |
Feb 25, 2021 |
| Last update date |
Sep 23, 2022 |
| Contact name |
Kiran Mahajan |
| E-mail(s) |
kiranm@wustl.edu
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| Phone |
3142737728
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| Organization name |
Washington University
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| Department |
Surgery
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| Lab |
Kiran Mahajan Lab
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| Street address |
CB 8242 600 South Euclid Ave
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| City |
St. Louis |
| State/province |
Missouri |
| ZIP/Postal code |
63110 |
| Country |
USA |
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| Platforms (1) |
| GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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| Samples (1) |
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| Relations |
| BioProject |
PRJNA704829 |
| SRA |
SRP308165 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE167506_RAW.tar |
31.9 Mb |
(http)(custom) |
TAR (of H5) |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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