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Series GSE201770 Query DataSets for GSE201770
Status Public on Sep 14, 2023
Title Lysine methylation of EHMT1/GLP as a molecular switch to reprogram transcription networks in prostate cancer [RNA-seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Our studies provide novel molecular insights into the activity and function of EHMT1 during PCa progression and suggest a novel therapeutic strategy to treat CRPC with EHMT1 inhibitors.
 
Overall design LNCaP-tet-EHMT1 cells were treated with/out 0.25ug/mL doxycycline for two days. LNCaP cells were treated with siNTC, siEHMT1 at 20nM for two days. All RNA-seq samples contain replications.
 
Contributor(s) Besschetnova A, Han W, Liu M, Han D, Cai C
Citation(s) 37663929
Submission date Apr 28, 2022
Last update date Sep 14, 2023
Contact name Changmeng Cai
E-mail(s) changmeng.cai@umb.edu
Organization name University of Massachusetts Boston
Street address 100 William T Morrissey Blvd
City Boston
State/province MA
ZIP/Postal code 02125
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (20)
GSM6071082 siNTC-rep 1
GSM6071083 siNTC-rep 2
GSM6071084 siEHMT1-rep 1
This SubSeries is part of SuperSeries:
GSE201771 Lysine methylation of EHMT1/GLP as a molecular switch to reprogram transcription networks in prostate cancer
Relations
BioProject PRJNA832968

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE201770_LNCaP_EHMT1_count_table.txt.gz 957.6 Kb (ftp)(http) TXT
GSE201770_LNCaP_siEHMT1_count_table.txt.gz 613.6 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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