|
Status |
Public on Mar 09, 2017 |
Title |
MCF7_DMSO_2 |
Sample type |
SRA |
|
|
Source name |
MCF-7 breast cancer cells
|
Organism |
Homo sapiens |
Characteristics |
cell line: MCF7 treatment: DMSO
|
Treatment protocol |
Samples 1-8. MCF-7 cells that had been lentivirally infected with constructs for inducible expression of small hairpin RNA's directed against the MEN1 mRNA (ShMEN1#1) or a control sequence (ShCtrl) were synchronized for 72 hrs in phenol red-free medium (DMEM) containing 10% charcoal dextran-treated fetal bovine serum (CDT medium). Expression of small hairpin RNA's was induced by adding 100 ng/ml doxycycline for 72 hrs. 10nM estradiol or vehicle was added to the cells for 45 mins. Samples 9-12. MCF-7 cells were treated with 1mM of the menin inhibitor MI-2 or DMSO for 4 days.
|
Growth protocol |
Cells were maintained at 37oC and 5% CO2 in DMEM + 10% FBS and Pen-Strep.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using RNeasy Libraries were made from total RNA using the Illumina TruSeq Stranded mRNA Library Prep Kit
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
Expression_transcripts_MI2.txt
|
Data processing |
Basecalls were performed with FastQC version 0.10.0. RNA-seq reads were aligned to the hg19 genome assembly using Tophat Genome_build: hg19
|
|
|
Submission date |
Aug 31, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Koen M.A. Dreijerink |
E-mail(s) |
koendreijerink@yahoo.com
|
Organization name |
Dana-Farber Cancer Institute
|
Department |
Medical Oncology
|
Street address |
450 Brookline Avenue
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
|
|
Platform ID |
GPL18573 |
Series (1) |
GSE86316 |
Messenger RNA expression after silencing or inhibition of MEN1in MCF-7 breast cancer cells |
|
Relations |
BioSample |
SAMN05721616 |
SRA |
SRX2071020 |