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Sample GSM325268 Query DataSets for GSM325268
Status Public on Oct 06, 2008
Title Patient no. 11: control
Sample type RNA
 
Source name Liposarcoma culture from tumor 389, untreated
Organism Homo sapiens
Characteristics Sex: female
Age at operation: 57 years
Site: thorax
Size in cm: 4.9x4x3
Histological Subtype: pleomorphic liposarcoma
Responder type: high
Grading: G3
Specimen character: local recurrence
Previous radiation: no
Previous chemotherapy: no
Treatment protocol 24 h later, after having grown to a subconfluent layer, cell cultures were incubated with doxorubicin (0.5 ug/ml) for 24 h or an equal volume of PBS as control
Growth protocol Primary human liposarcoma cultures were isolated by dissecting the tumor and digesting the minced samples enzymatically with 10 ml each of collagenase and dispase (10 mg/ml). The single cell suspension was depleted of red blood cells and cellular debris by centrifugation through a Ficoll-Hypaque density gradient. Liposarcioma cells were diluted and cultured during the whole experiment with Leibovitz's L-15 medium, supplemented with 2.0 mM glutamine and 10% fetal bovine serum in a humidified atmosphere in free air exchange with atmospheric air. Cells were seeded at a density of 2.00E+06 in 25 cm2 flasks.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 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 Human Genome U133A Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description Gene expression data from primary liposarcom cultures incubated with PBS as control for 24 h
Data processing The data were analyzed with GCOS 1.4 using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 1000.
 
Submission date Sep 29, 2008
Last update date Jan 13, 2009
Contact name Ludger Klein-Hitpass
E-mail(s) ludger.klein-hitpass@uni-essen.de
Phone +49 201 723 85552
Organization name Institut fuer Zellbiologie
Department Universitaetsklinikum
Lab BioChip Lab
Street address Virchowstr. 173
City Essen
ZIP/Postal code D-45122
Country Germany
 
Platform ID GPL96
Series (1)
GSE12972 Heterogeneous in vitro effects of doxorubicin on gene expression in primary human liposarcoma cultures

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 1105.12 P 0.00110197
AFFX-BioB-M_at 2031.33 P 8.14279e-05
AFFX-BioB-3_at 697.815 P 0.00141043
AFFX-BioC-5_at 3330.06 P 6.02111e-05
AFFX-BioC-3_at 1869.78 P 7.00668e-05
AFFX-BioDn-5_at 2013.42 P 7.00668e-05
AFFX-BioDn-3_at 13696.3 P 7.00668e-05
AFFX-CreX-5_at 27893.5 P 4.42873e-05
AFFX-CreX-3_at 41455.3 P 4.42873e-05
AFFX-DapX-5_at 1110.61 P 5.16732e-05
AFFX-DapX-M_at 2629.46 P 0.000753643
AFFX-DapX-3_at 2181.32 P 7.00668e-05
AFFX-LysX-5_at 19428.5 P 4.42873e-05
AFFX-LysX-M_at 27824 P 4.42873e-05
AFFX-LysX-3_at 42881.3 P 4.42873e-05
AFFX-PheX-5_at 33100.6 P 4.42873e-05
AFFX-PheX-M_at 37855.5 P 4.42873e-05
AFFX-PheX-3_at 47792.9 P 4.42873e-05
AFFX-ThrX-5_at 6316.86 P 4.42873e-05
AFFX-ThrX-M_at 8219.64 P 4.42873e-05

Total number of rows: 22283

Table truncated, full table size 672 Kbytes.




Supplementary file Size Download File type/resource
GSM325268.CEL.gz 3.2 Mb (ftp)(http) CEL
GSM325268.CHP.gz 117.4 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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