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Sample GSM1351769 Query DataSets for GSM1351769
Status Public on Apr 15, 2015
Title Patient 12 NCCRI_2012-054_24
Sample type RNA
 
Source name non-responder_primary lung cancer
Organism Homo sapiens
Characteristics subject id: Patient 12
therapeutic response: non-responder
gender: Female
age (yrs): 66
tissue: primary lung cancer
pathological type: adenocarcinoma (AD)
pathological stage: IIIA
Treatment protocol Twenty-nine patients who received four or more courses of first-line platinum-based chemotherapy after postoperative recurrence were divided into two groups (responder (n=17) and non-responder group (n=12)).
Growth protocol Total RNA was extracted from human lungs using QIAzol and the miRNeasy Mini Kit (Qiagen) according to the manufacturer’s protocol. The purity and concentration of all RNA samples were quantified using NanoDrop ND-1000 (Thermo Scientific). Detection of RNA from human lungs was performed using the Agilent Bioanalyzer 2100 (Agilent Technologies, Santa Clara, CA). Prior to the analysis, total RNA was prepared with the Agilent RNA 6000 Pico kit (Agilent Technologies) according to the manufacturer’s protocol. All clinical samples exhibited RNA Integrity Numbers > 6.0.
Extracted molecule total RNA
Extraction protocol RNA samples were extracted from cells using miRNesy mini kit (Quiagen).
Label Hy5
Label protocol Extracted total RNA was labeled with Hy5 using the miRCURY LNA Array miR labeling kit (Exiqon, Vedbaek, Denmark)
 
Hybridization protocol Hybridized for 16 h at 37 C with rotary shake (250 rpm). Hybridization buffer and washing protocol was followed by the protocol supplied by TORAY Industries, Inc..
Scan protocol 3D-Gene Scanner ((Toray Industries Inc., Tokyo, Japan) was used for scanning. Images were quantified using Extraction(Toray Industries Inc., Tokyo, Japan).
Data processing The raw data of each spot was normalized by substitution with a mean intensity of the background signal determined by all blank spots’ signal intensities of 95% confidence intervals. Measurements of both duplicate spots with the signal intensities greater than 2 standard deviations (SD) of the background signal intensity were considered to be valid. A relative expression level of a given miRNA was calculated by comparing the signal intensities of the averaged valid spots with their mean value throughout the microarray experiments.
 
Submission date Mar 19, 2014
Last update date Apr 15, 2015
Contact name Satoshi Kondo
Organization name Toray Industries,Inc.
Department New Projects Development Division
Street address Tebiro 6-10-1
City Kamakura
State/province Kanagawa
ZIP/Postal code 248-8555
Country Japan
 
Platform ID GPL15446
Series (1)
GSE56036 microRNA microarray on a cohort study of platinum-sensitive versus platinum-resistant NSCLC patients

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
MIMAT0000062 5273.617888
MIMAT0000063 2240.858102
MIMAT0000064 4725.561979
MIMAT0000065 3297.549279
MIMAT0000066 1289.757592
MIMAT0000067 4198.221963
MIMAT0000068 970.085316
MIMAT0000069 2139.365598
MIMAT0000070 2325.474307
MIMAT0000071 207.10902
MIMAT0000072 337.975347
MIMAT0000073 775.094262
MIMAT0000074 4703.385586
MIMAT0000075 2082.416204
MIMAT0000076 44460.16531
MIMAT0000077 2225.002312
MIMAT0000078 10799.99099
MIMAT0000079 19.770545
MIMAT0000080 5080.783361
MIMAT0000081 263.821843

Total number of rows: 1719

Table truncated, full table size 35 Kbytes.




Supplementary file Size Download File type/resource
GSM1351769_PH27224-1.txt.gz 158.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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