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Status |
Public on Jan 05, 2015 |
Title |
The placental gene PEG10 promotes progression of neuroendocrine prostate cancer [aCGH] |
Organism |
Homo sapiens |
Experiment type |
Genome variation profiling by genome tiling array
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Summary |
Neuroendocrine prostate cancer (NEPC) is proliferative, invasive, and untreatable. Its molecular pathogenesis remains poorly understood but appears to require TP53 and RB1 aberration. In this study we modeled the development of NEPC from conventional prostatic adenocarcinoma using a unique patient-derived xenograft and identified up-regulation of the placental gene PEG10. We found that the androgen receptor and the E2F/RB pathway dynamically regulate distinct post-transcriptional and post-translational isoforms of PEG10 at different stages of NEPC development. In vitro, PEG10 promoted cell cycle progression from G0/G1 in the context of TP53 loss, and regulated Snail expression via TGF-β signaling to promote invasion. Finally we show in vivo proof of principal using antisense oligonucleotide that PEG10 is a novel therapeutic target for NEPC.
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Overall design |
Six patient-derived xenograft tumors from the LTL331 xenograft lineage (PMID: 24356420; http://www.livingtumorcentre.com/) after differing lengths of time post-host castration. No replicates.
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Contributor(s) |
Wyatt AW, Collins CC |
Citation(s) |
29757368 |
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Submission date |
Jul 31, 2014 |
Last update date |
Jul 26, 2019 |
Contact name |
Shawn Anderson |
E-mail(s) |
[email protected]
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Organization name |
Vancouver Prostate Centre
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Lab |
Laboratory for Advanced Genome Analysis
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Street address |
2660 Oak Street
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City |
Vancouver |
State/province |
BC |
ZIP/Postal code |
V6H3Z6 |
Country |
Canada |
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Platforms (1) |
GPL10152 |
Agilent-021924 SurePrint G3 Human CGH Microarray 8x60K (Feature Number version) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE59986 |
The placental gene PEG10 promotes progression of neuroendocrine prostate cancer |
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Relations |
BioProject |
PRJNA257215 |