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Sample GSM325276 Query DataSets for GSM325276
Status Public on Oct 06, 2008
Title Patient no. 2: control
Sample type RNA
 
Source name Liposarcoma culture from tumor 337, untreated
Organism Homo sapiens
Characteristics Sex: female
Age at operation: 74 years
Site: thigh
Size in cm: 14.5x7.5x9
Histological Subtype: myxoid/roundcell liposarcoma
Responder type: high
Grading: G3
Specimen character: primary tumor
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 604.365 P 0.00110197
AFFX-BioB-M_at 1337.68 P 0.000126798
AFFX-BioB-3_at 418.682 P 0.0020226
AFFX-BioC-5_at 1917 P 7.00668e-05
AFFX-BioC-3_at 1358.33 P 5.16732e-05
AFFX-BioDn-5_at 1316.06 P 7.00668e-05
AFFX-BioDn-3_at 10451.4 P 0.000169227
AFFX-CreX-5_at 17908.5 P 4.42873e-05
AFFX-CreX-3_at 25753.6 P 4.42873e-05
AFFX-DapX-5_at 283.303 P 0.000258358
AFFX-DapX-M_at 644.677 P 0.0032123
AFFX-DapX-3_at 675.169 P 0.0012475
AFFX-LysX-5_at 3743.36 P 4.42873e-05
AFFX-LysX-M_at 5496.65 P 4.42873e-05
AFFX-LysX-3_at 8683.65 P 4.42873e-05
AFFX-PheX-5_at 9386.52 P 4.42873e-05
AFFX-PheX-M_at 10852.6 P 4.42873e-05
AFFX-PheX-3_at 9986.11 P 4.42873e-05
AFFX-ThrX-5_at 1790.79 P 5.16732e-05
AFFX-ThrX-M_at 2034.86 P 4.42873e-05

Total number of rows: 22283

Table truncated, full table size 673 Kbytes.




Supplementary file Size Download File type/resource
GSM325276.CEL.gz 3.4 Mb (ftp)(http) CEL
GSM325276.CHP.gz 117.4 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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