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Sample GSM1314323 Query DataSets for GSM1314323
Status Public on Jan 25, 2014
Title C_HP+_S08-5858
Sample type RNA
Source name H. pylori-positive FFPE specimen
Organism Homo sapiens
Characteristics disease: H. pylori-positive FFPE specimen (cancerous region)
tissue: FFPE specimen
Treatment protocol All subjects of this study received gastroscopy for gastric cancer screening and conformation of histological gastric adenocarcinoma diagnosis.
Growth protocol Sixteen gastric cancer patients matched for age, sex and H. pylori status, who received curative operation at Seoul National University Bundang Hospital, were included for microarray study.
Extracted molecule total RNA
Extraction protocol After manual dissection under microscopic guidance avoiding the contamination of inflammatory cells and stromal cells, H&E stained sections 50 μm in thickness from cancerous and non-cancerous regions of intestinal type of gastric cancer FFPE samples were reviewed by one pathologist (H.S.L). Each section was incubated in xylene and total RNA was extracted using a RecoverAllTM Total Nucleic Acid Isolation kit (Life Technologies, CA, USA).
Label Cy3
Label protocol 400 ng of total RNA was labeled with cyanine 3-pCp using the Agilent miRNA Complete Labeling kit and hybridized to the array according to the manufacturer’s protocol.
Hybridization protocol After purification, labeled samples were resuspended with Gene Expression Blocking Reagent and Hi-RPM Hybridization buffer, followed by boiling for 5 min at 100 °C and 5 min chilled on ice. Finally, denatured labeled probes were pipetted onto assembled Agilent’s Human miRNA Microarray (60K, Release 16.0) and hybridized at 55 °C for 20 h with 20 rpm rotating in Agilent Hybridization Oven. The hybridized microarrays were washed as the manufacturer’s washing protocol (Agilent Technology).
Scan protocol The hybridization images were analyzed by Agilent DNA microarray Scanner.
Description miRNA expression in the H. pylori-positive FFPE specimen (cancerous region), C_HP+_S08-5858
Data processing Feature Extraction software (version was used for data extraction from raw microarray image files using the miRNA_105_Dec08 FE protocol. Background intensity and feature nonuniform outliers were removed by standard procedures. Data visualization and analysis were performed with GeneSpring GX (version 7.3) software (Agilent Technologies). Signal cut-off measurements were less than 5, and normalized to 75th percentile of signal intensity to standardize each chip for cross-array comparison. Differentially expressed miRNAs were identified using a Student’s two-sample t-test with p values cut off by 0.05 and fold change more than 2.0. One-way ANOVO was used to analyze the correlation between the expression levels of miRNAs and clinic-pathological features of the patients.
Submission date Jan 24, 2014
Last update date Jan 25, 2014
Contact name Jung Min Kim
Phone 82-10-3459-4776
Organization name NAR Center, Inc. & Genoplan, Inc.
Department Department of Health Genomics
Lab Genetics & Genomics
Street address Gangnam-gu Teheran-ro 216
City Seoul
ZIP/Postal code 06221
Country South Korea
Platform ID GPL15159
Series (1)
GSE54397 microRNA expressions in gastric cancer

Data table header descriptions
VALUE Normalized signal intensity

Data table
A_25_P00010019 6.101282
A_25_P00010020 1.3085518
A_25_P00010021 -0.0953272
A_25_P00010023 1.5617567
A_25_P00010041 -1.6100489
A_25_P00010042 -0.5387885
A_25_P00010043 -1.3495436
A_25_P00010044 -1.3365376
A_25_P00010047 212.9177
A_25_P00010048 38.24137
A_25_P00010053 1163.3046
A_25_P00010054 193.74036
A_25_P00010062 12.171408
A_25_P00010063 2.2846186
A_25_P00010070 9230.808
A_25_P00010071 6057.4673
A_25_P00010072 3664.3567
A_25_P00010073 744.5531
A_25_P00010078 513.36084
A_25_P00010079 115.408485

Total number of rows: 3523

Table truncated, full table size 86 Kbytes.

Supplementary file Size Download File type/resource
GSM1314323_C_HP+_S08-5858.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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