|
| Status |
Public on Apr 23, 2018 |
| Title |
Genome wide analysis of androgen-receptor binding sites and associated factors in prostate cancer cells |
| Organism |
Homo sapiens |
| Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
| Summary |
Prostate cancer is the most common cancer in men and AR downstream signalings promote prostate cancer cell proliferation. To investigate the AR signaling, we performed ChIP sequence analysis in AR positive prostate cancer cell line, LNCaP and VCaP. In addition, we used hormone-refractory prostate cancer model cells, long term androgen deprivation (LTAD) to explore the differences of androgen signaling in prostate cancer progression.
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| |
|
| Overall design |
ChIP sequence analysis of AR binding sites, assocaited factors and epigenetic condition in two prostate cancer cells
|
| |
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| Contributor(s) |
Takayama K |
| Citation(s) |
29686105 |
| Submission date |
Feb 06, 2017 |
| Last update date |
May 21, 2019 |
| Contact name |
Ken-ichi Takayama |
| Organization name |
Tokyo Metropolitan Institute of Gerontology
|
| Street address |
Sakaecho
|
| City |
Itabashi-ku |
| ZIP/Postal code |
173-0015 |
| Country |
Japan |
| |
|
| Platforms (2) |
| GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
| GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
|
| Samples (32)
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| Relations |
| BioProject |
PRJNA371492 |
| SRA |
SRP098935 |
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