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Sample GSM4907445 Query DataSets for GSM4907445
Status Public on Nov 13, 2023
Title progression_CRLM8_1
Sample type RNA
 
Source name human leiomyoma
Organism Homo sapiens
Characteristics treatment: cadmium-treated
Sex: female
cell type: human uterine leiomyoma cell line immortalized via retroviral transfection of telemorase (ht-UtLM)
Treatment protocol For 8-week Cd-exposure experiment, the ht-UtLM cultures were maintained continuously in ht-UtLM culture medium supplemented with 10 μM CdCl2 for 8 weeks. The culture medium was replaced with fresh medium with 10 μM CdCl2 every 3 days. Passage-matched control ht-UtLM cultures were run concurrently with Cd exposed cells. All cultures were kept in a standard tissue culture incubator at 37°C with 5% CO2.
Growth protocol A human uterine leiomyoma cell line immortalized via retroviral transfection of telemorase (ht-UtLM) was generated by our laboratory. Human fibroblast and vulvar leiomyosarcoma (SKS-LMS-1) cell lines were cultured in DMEM medium supplemented with 10% FBS. All cultures were kept in a standard tissue culture incubator at 37°C with 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated by extracting with Trizol ™ Reagent (ThermoFisher Cat# 15596026) and subsequently purifying with an Rneasy Mini Kit (Qiagen Cat#74104).
Label na
Label protocol n/a
 
Hybridization protocol Reporter and Capture probes were added according to the manufacturer’s directions (nanostring.com) to 50 ng of total RNA in a final volume of 15ul followed by hybridization for at least 14 hours at 65oC
Scan protocol After sample processing according to manufacturer’s instructions on the nCounter Prep Station Model 5S, sample cartridges were scanned on an nCounter Digital Analyzer Model 5S, using 555 Fields of Vision (FOV) and the .rlf file 'NS_Cancerprog_C4972'.
Description Immortalized human leiomyoma cells, female, benign tumor, age unknown.
Data processing Data were adjusted utilizing the manufacturer's positive and negative control probes, as well as internal housekeeping genes. This nSolver adjusted data were then imported into Partek(v7.0), log2 transformed and quantile normalized.
 
Submission date Nov 13, 2020
Last update date Nov 13, 2023
Contact name Rick David Fannin
E-mail(s) fannin@niehs.nih.gov
Phone 9842874069
Organization name Mr.
Department NIEHS/NIH
Lab Genomics Core
Street address 111 Tw Alexander Dr, MD D204
City RTP
State/province NC
ZIP/Postal code 27709
Country USA
 
Platform ID GPL26599
Series (2)
GSE161454 The effects of the prolonged Cd exposure on gene expression changes in in Uterine Leiomyoma Cells [cancer progression]
GSE161456 The effects of the prolonged Cd exposure on gene expression changes in in Uterine Leiomyoma Cells

Data table header descriptions
ID_REF
VALUE Values are direct ‘counts’ of the number of gene specific epifluorescant dye barcodes in the scanned image.

Data table
ID_REF VALUE
AAMP 444.31
ABI3BP 546.79
ACHE 12.48
ACTG2 12.48
ACVR1 665.65
ACVR1C 22.13
ACVRL1 12.48
ADAM15 406.61
ADAM17 184.45
ADAM28 12.48
ADAM8 12.48
ADAM9 2202.72
ADAMTS1 5378.5
ADAMTS12 12.48
ADAMTS8 12.48
ADAP1 12.48
ADD1 1250.15
ADM2 12.48
ADRA2B 13.94
AEBP1 12.48

Total number of rows: 784

Table truncated, full table size 9 Kbytes.




Supplementary file Size Download File type/resource
GSM4907445_20181128_Nano97car1_CR1_04.RCC.gz 8.6 Kb (ftp)(http) RCC
Processed data included within Sample table

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