NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM651855 Query DataSets for GSM651855
Status Public on Feb 15, 2011
Title Cervical cancer-lymph node positive-25-10
Sample type RNA
 
Source name Early stage cervical cancer
Organism Homo sapiens
Characteristics pelvic lymph nodes: Positive
age at diagnosis: 49.9
figo stage: 2a
Treatment protocol Primary treatment consisted of type 3 radical hysterectomy and pelvic lymph node dissection. In case of poor prognostic factors, such as lymph node metastases or positive resection margins, patients were treated with adjuvant radiotherapy or chemoradiation.
Extracted molecule total RNA
Extraction protocol From the frozen biopsies, four 10 mm thick sections were cut and used for standard RNA isolation. After cutting, a 3 mm thick section was stained with hematoxylin/eosin for histological examination and only tissues with >80% tumor cells were included. RNA was isolated with TRIzol reagent (Invitrogen, Breda, the Netherlands) according to manufacturer's protocol. RNA was treated with DNAse and purified using the RNeasy mini-kit (Qiagen, Westburg, Leusden, the Netherlands). The quality and quantity of the RNA was determined by Agilent Lab-on-Chip analysis.
Label Biotin
Label protocol For labelling, 10 μg of total RNA was amplified by in vitro transcription using T7 RNA polymerase, according to standard Affymetrix protocols.
 
Hybridization protocol Labelled RNA samples were hybridized according to a randomized design to the human genome U133 plus 2.0 microarrays (Affymetrix, Santa Clara, CA). The microarrays were loaded with 200 μl of hybridization cocktail solution and then placed in Genechip Hybridization Oven 640 (Affymetrix) rotating at 60 rpm at 45 °C for 16 h.
Scan protocol After hybridization, the arrays were washed on Genechip Fluidics Station 400 (Affymetrix) and scanned using Genechip Scanner 3000 (Affymetrix) according to the manufacturers’ procedure. Labeling of the RNA, quality control, the microarray hybridization and scanning were performed by ServiceXS (Leiden, the Netherlands ) according to Affymetrix standards.
Description Gene expression data from cervical cancer tissue of patient with pelvic lymph node metastasis
Data processing Processing of CEL files was performed with Affymetrix Expression Console software. Probe set expression summary was done using the Robust Multi-array Average (RMA) algorithm. Quality of the microarray data was checked using histograms, box plots and a RNA degradation plot. Principal component analysis (PCA) was performed for controlling the quality of the hybridizations.
 
Submission date Jan 10, 2011
Last update date Feb 15, 2011
Contact name Maartje Noordhuis
E-mail(s) m.noordhuis@og.umcg.nl
Organization name University Medical Center Groningen
Department Gynecologic Oncology
Street address PObox 30.001
City Groningen
ZIP/Postal code 9700RB
Country Netherlands
 
Platform ID GPL570
Series (1)
GSE26511 Involvement of the TGF-β and β-catenin pathways in pelvic lymph node metastasis in early stage cervical cancer

Data table header descriptions
ID_REF
VALUE Gene expressions were normalized and log-transformed

Data table
ID_REF VALUE
AFFX-BioB-5_at 7.3344
AFFX-BioB-M_at 7.7474
AFFX-BioB-3_at 6.87411
AFFX-BioC-5_at 8.21375
AFFX-BioC-3_at 8.22767
AFFX-BioDn-5_at 8.50317
AFFX-BioDn-3_at 11.0917
AFFX-CreX-5_at 11.8431
AFFX-CreX-3_at 12.4777
AFFX-DapX-5_at 4.16709
AFFX-DapX-M_at 3.86963
AFFX-DapX-3_at 4.18359
AFFX-LysX-5_at 3.54296
AFFX-LysX-M_at 4.80321
AFFX-LysX-3_at 5.23961
AFFX-PheX-5_at 4.00575
AFFX-PheX-M_at 3.86629
AFFX-PheX-3_at 5.90625
AFFX-ThrX-5_at 4.48969
AFFX-ThrX-M_at 3.96183

Total number of rows: 54675

Table truncated, full table size 998 Kbytes.




Supplementary file Size Download File type/resource
GSM651855.CEL.gz 8.7 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap