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Sample GSM4121428 Query DataSets for GSM4121428
Status Public on Oct 16, 2019
Title S1-3D TC
Sample type RNA
 
Source name S1 cells embedded and grown in 3D rBM and treated with TRAIL
Organism Homo sapiens
Characteristics tissue: breast epithelium
Treatment protocol Cells were pre-treated with caspase inhibitors DEVD-CHO and Ac-IETD-CHO (1μM, respectively) at least 2 hours before TRAIL treatment (1 ug/ml) for 8hrs.
Growth protocol HMT-3522 S1 cells were propagated as monolayers on rBM-coated tissue culture plastics in chemically defined medium comprising of DMEM/F12, prolactin (0.15 IU/ml), insulin (250 ng/ml), hydrocortisone (1.4 μM), sodium selenite (2.6 ng/ml), β-Estradiol (0.1 nM), Apo-transferrin (10 μg/ml), and EGF (10 ng/ml). For 3D culture, S1 cells were embedded in 3D rBM (Matrigel, BD Bioscience) and grown for 12 days to form 3D acini organoids before the subsequent treatment.
Extracted molecule total RNA
Extraction protocol TRIzol extraction of total RNA was performed according to the manufacturer's instructions. The resulted RNA samples were further purified by Rneasy Mini Kit (Qiagen).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol Arrays were scanned by a confocal scanner.
Description S1 cells were embedded in 3D rBM and treated with TRAIL (1ug/ml) for 8 hours, replication 3.
Data processing Affymetrix .cel files were processed with ArrayAssist Lite (v3.4, Stratagene). The files were imported and processed with the GC-RMA algorithm to yield probe set intensities and additionally, Affymetrix Preset, Absent, Marginal flags were computed. These values were exported in .chp files, which were subsequently imported into the Partek Genomics Suite software (v6.2).
 
Submission date Oct 15, 2019
Last update date Oct 16, 2019
Contact name Kelvin Kun-Chih Tsai
Organization name Taipei Medical University
Department Graduate Institute of Clinical Medicine, College of Medicine
Lab Laboratory of Advanced Molecular Therapeutics
Street address 7F, 250 Wuxing St, Xinyi Dist
City Taipei City
ZIP/Postal code 11031
Country Taiwan
 
Platform ID GPL96
Series (1)
GSE138900 Gene expression profile of HMT3522 S1 cells grown on 2D and in 3D matrix in response to the death ligand TRAIL

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 227.615 P 0.00255552
AFFX-BioB-M_at 272.924 P 0.000126798
AFFX-BioB-3_at 201.759 P 9.4506e-05
AFFX-BioC-5_at 701.185 P 9.4506e-05
AFFX-BioC-3_at 704 P 4.42873e-05
AFFX-BioDn-5_at 1232.41 P 4.42873e-05
AFFX-BioDn-3_at 3415.64 P 7.00668e-05
AFFX-CreX-5_at 6446.72 P 4.42873e-05
AFFX-CreX-3_at 10513.3 P 5.16732e-05
AFFX-DapX-5_at 2.49973 A 0.9273
AFFX-DapX-M_at 6.63551 A 0.60308
AFFX-DapX-3_at 8.9662 A 0.699394
AFFX-LysX-5_at 13.1239 A 0.51489
AFFX-LysX-M_at 5.40056 A 0.932322
AFFX-LysX-3_at 19.835 A 0.327079
AFFX-PheX-5_at 4.83386 A 0.804734
AFFX-PheX-M_at 1.65684 A 0.984817
AFFX-PheX-3_at 6.1478 A 0.814869
AFFX-ThrX-5_at 8.2063 A 0.783476
AFFX-ThrX-M_at 4.20923 A 0.904333

Total number of rows: 22283

Table truncated, full table size 665 Kbytes.




Supplementary file Size Download File type/resource
GSM4121428_S1-3D_TC.CEL.gz 1.9 Mb (ftp)(http) CEL
GSM4121428_S1-3D_TC.CHP.gz 2.6 Mb (ftp)(http) CHP
Processed data provided as supplementary file
Processed data included within Sample table

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