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Sample GSM1405680 Query DataSets for GSM1405680
Status Public on Jul 29, 2016
Title G2911_HumanHodgkinLymphoma-HamsterHybridTumorGW-532_generation 2
Sample type RNA
 
Source name GW-532
Organism Homo sapiens
Characteristics hybrid: : Homo sapiens-Mesocricetus auratus hybrids
original tumor type: Hodgkin lymphoma
sample type: FFPE
Treatment protocol Tissue samples were preserved as formalin-fixed paraffin-embedded (FFPE) tissue blocks for up to 40 years and sectioned to 5-10 um thick for nucleic acid isolation.
Growth protocol Various human tumors were inidividually grafted to the cheek pouches of adult, unconditioned golden hamsters (Mesocricetus auratus), and the resulting tumor for each was serially passaged in hamsters for multiple years.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNeasy FFPE Kit (Qiagen, Germantown, MD) according to manufacturer’s instructions (3h incubation at 55 degrees C followed by glass fiber filtration). RNA purity was checked by OD260/280 readings and RNA integrity was checked using Agilent Bioanalyzer capillary electrophoresis profiles.
Label biotin
Label protocol Biotinylated cDNA from each sample weas prepared by conversion of 50 ng total RNA to cDNA by reverse transcription, amplification by the SPIA method, and fragmentation and labeling with biotin using the Ovation Pico WTA System v2 and Encore Biotin Module kits according to the manufacturer’s instructions (NuGEN, San Carlos CA).
 
Hybridization protocol 5.5 ug of fragmented, biotin-labeled cDNA were hybridized for 16 hr at 45 degrees C on GeneChip Human U133_X3P arrays (Affymetrix; catalog no. 900516). GeneChips were washed and stained with streptavidin-phycoerythrin using the Affymetrix Fluidics Station 450, according to the manufacturer's recommended protocol.
Scan protocol GeneChips were scanned using the Affymetrix GCS 3000 7G.
Description GW-532: A male’s left axillary Hodgkin lymphoma containing Hodgkin Reed Sternberg (HRS) cells was grafted to the cheek pouches of adult, unconditioned golden hamsters (Mesocricetus auratus), and the resulting tumor was serially passaged in hamsters for >6 years. The transplants were morphologically similar to portions of the original donor specimen, even with HRS cells being identified as early as 17 days after the initial transplantation. This and all subsequent transplant generations showed widespread metastases from the cheek pouch grafts. This sample was obtained from transplant generation 2.
Data processing Fluorescent signals were collected and processed by AGCC and MAS 5.0 using Affymetrix default analysis settings and global scaling as the normalization method in Expression Colsole. The trimmed mean target intensity (TGT) of each array was set to 250. Following MAS 5.0 normalization and global scaling, unannotated probe sets and probe sets for which no signal value was greater than the median signal for AFFX spike-in controls with all Absent Detection Calls were omitted from further analysis. Subsequently, because an intact hamster cell line (sample IMM006, cell line CCL-49) control RNA sample was used for comparison with the four human-hamster hybrid FFPE samples, all remaining signal values for the hamster cell line sample were multiplied by the ratio of the median signal in all FFPE hybrid samples for AFFX spike-in control probe sets called present in all samples divided by the median signal for the same probe sets in the hamster control sample.
 
Submission date Jun 06, 2014
Last update date Jul 29, 2016
Contact name David M Goldenberg
E-mail(s) dmg.gscancer@att.net
Organization name Garden State Cancer Center
Department Center for Molecular Medicine and Immunology
Street address 300 The American Road
City Morris Plains
State/province NJ
ZIP/Postal code 07950
Country USA
 
Platform ID GPL1352
Series (1)
GSE58277 In-Vivo Fusion of Human Cancer and Hamster Stromal Cells Permanently Transduces and Transcribes Human DNA

Data table header descriptions
ID_REF
VALUE MAS5.0 signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
1053_3p_at 612.4619 A 0.6974525
117_3p_at 1174.978 A 0.1759894
1494_3p_f_at 1150.087 A 0.0980541
1552275_3p_s_at 45.06305 A 0.8508301
1552281_3p_at 1213.493 A 0.219482
1552296_3p_at 636.1597 A 0.533936
1552302_3p_at 200.5529 A 0.366211
1552311_3p_a_at 4412.003 A 0.27417
1552321_3p_a_at 74.75842 A 0.943848
1552340_3p_at 601.3416 A 0.27417
1552343_3p_s_at 521.2371 A 0.398926
1552354_3p_at 136.0824 A 0.850342
1552476_3p_s_at 204.4421 A 0.932373
1552480_3p_s_at 48.0675 A 0.962402
1552504_3p_a_at 154.4629 A 0.665527
1552518_3p_s_at 319.7766 A 0.633789
1552528_3p_at 132.1713 A 0.870361
1552535_3p_at 155.635 A 0.533936
1552566_3p_at 171.2465 A 0.9296875
1552575_3p_a_at 77.13868 A 0.888428

Total number of rows: 46123

Table truncated, full table size 1771 Kbytes.




Supplementary file Size Download File type/resource
GSM1405680_IMM001-U133_X3P.CEL.gz 3.4 Mb (ftp)(http) CEL
GSM1405680_IMM001-U133_X3P.mas5.CHP.gz 649.2 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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