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Sample GSM325245 Query DataSets for GSM325245
Status Public on Oct 06, 2008
Title Patient no. 18: treated
Sample type RNA
 
Source name Liposarcoma culture from tumor 400, doxorubicin treated
Organism Homo sapiens
Characteristics Sex: female
Age at operation: 67 years
Site: thigh
Size in cm: 35x15x12
Histological Subtype: atypical lipoma
Responder type: low
Grading: G1
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 doxorubicin (0.5 µg/ml) 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 1221.93 P 0.000753643
AFFX-BioB-M_at 1942.84 P 9.4506e-05
AFFX-BioB-3_at 768.574 P 0.000258358
AFFX-BioC-5_at 2856.67 P 0.000126798
AFFX-BioC-3_at 1983.93 P 4.42873e-05
AFFX-BioDn-5_at 3116.72 P 4.42873e-05
AFFX-BioDn-3_at 16724.6 P 7.00668e-05
AFFX-CreX-5_at 27105.6 P 4.42873e-05
AFFX-CreX-3_at 43822.7 P 4.42873e-05
AFFX-DapX-5_at 971.048 P 0.000126798
AFFX-DapX-M_at 2461.48 P 0.000753643
AFFX-DapX-3_at 2834.12 P 8.14279e-05
AFFX-LysX-5_at 7628.21 P 4.42873e-05
AFFX-LysX-M_at 11716.5 P 4.42873e-05
AFFX-LysX-3_at 20756.1 P 4.42873e-05
AFFX-PheX-5_at 34791.8 P 4.42873e-05
AFFX-PheX-M_at 38911.2 P 4.42873e-05
AFFX-PheX-3_at 47844.5 P 4.42873e-05
AFFX-ThrX-5_at 6686.6 P 4.42873e-05
AFFX-ThrX-M_at 8540.73 P 4.42873e-05

Total number of rows: 22283

Table truncated, full table size 671 Kbytes.




Supplementary file Size Download File type/resource
GSM325245.CEL.gz 3.3 Mb (ftp)(http) CEL
GSM325245.CHP.gz 117.5 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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