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Sample GSM4711609 Query DataSets for GSM4711609
Status Public on Aug 05, 2023
Title 22Rv1Ctrl_untreated_rep1
Sample type RNA
 
Source name Prostate carcinoma epithelial cell line derived from a xenograft that was serially propagated in mice after castration-induced regression and relapse of the parental, androgen-dependent CWR22 xenograft
Organism Homo sapiens
Characteristics cell type: Prostate cancer cells
cell line: 22Rv1
genotype: NCOA6 wild type
treatment: Untreated
Treatment protocol The 22Rv1Ctrl cell line was established by transfecting 22Rv1Par. cells with PX459 plasmids to transiently express Cas9. The 22Rv1NCOA6KO #2-74, #2-96, #4-91 and #4-105 cell lines were established by transfecting 22Rv1Par. cells with constructed PX459 plasmids to transiently co-express Cas9 and sgRNA targeting the exon 5 or 6 of the NCOA6 gene. The transfected cells were cultured in RPMI 1640 complete medium containing 5 µg/ml puromycin (P8833; Sigma) for 2 days. Selected cells were seeded into 150 mm dishes at a density of 200 cells per dish to grow clones. Individual clones were picked up and expanded. Positive clones including the 22Rv1NCOA6KO #2-74, #2-96, #4-91 and #4-105 cell lines were identified by PCR-based genotyping, DNA sequencing, and Western blot analysis.
Growth protocol The 22Rv1-derived cell lines were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (10437028; Thermo Fisher) and 1% penicillin (10000 IU)/streptomycin (10000 µg/ml) solution (30-002-CI; Corning). Cells were maintained at 37°C in a 5% CO2 cell culture incubator.
Extracted molecule total RNA
Extraction protocol Total RNA samples were extracted from the 22Rv1-derived cell lines using the TRIzol reagent (15596018; Thermo Fisher) followed by purification with the RNeasy Mini Kit (74106; Qiagen) according to the manufacturer's instructions. Quality of the samples was checked by using the Nanodrop ND-1000 and Agilent Bioanalyzer Nano Chip.
Label Cy3
Label protocol 50 ng of total RNA sample that had passed the quality check was mixed with Agilent's RNA Spike-Ins. The samples were amplified and labeled with Cy3 by using the Agilent Quick Amp Labeling Kit (Agilent p/n 5190-2331) according to the protocol (version 6.7). As a result, the Cy3-labeled cRNA was generated. The cRNA samples were purified using Qiagen RNeasy mini spin columns. Yield and dye incorporation of the samples were measured on Nanodrop.
 
Hybridization protocol The samples were fragmented. 0.6 μg of the fragmented sample and hybridization mix was loaded onto each of the Agilent G3 Human Gene Expression v3 8x60K Expression arrays (G4851C). The slides were hybridized in Agilent Hybridization Chamber at 65°C at a rotation rate of 10 rpm for 17 hours. The hybridized slides were washed with the Agilent Expression Wash Buffer Set 1 and 2 as per the Agilent protocol.
Scan protocol Once dry, the slides were scanned with the Agilent Scanner (G2565BA) using Scanner Version C and Scan Control software (version A.8.5.1). Data extraction and quality assessment of the microarray data were performed using Agilent Feature Extraction Software (Version 11.0.1.1).
Description NCOA6 wild type
Data processing The Bioconductor “limma” package (http://bioconductor.org) was used to analyze the microarray data. The data background was corrected using the “normexp” method with an offset of 16 added to the intensities. The background-corrected data were then log2-transformed and quantile-normalized.
 
Submission date Aug 05, 2020
Last update date Aug 05, 2023
Contact name Yonghong Liu
E-mail(s) yonghongliu2017@gmail.com
Phone 7137984684
Organization name Baylor College of Medicne
Department Molecular & Cellular Biology
Lab N630
Street address One Baylor Plaza
City Houston
State/province Texas
ZIP/Postal code 77030
Country USA
 
Platform ID GPL21185
Series (2)
GSE155754 Identification of differentially expressed genes influenced by NCOA6 in 22Rv1 human prostate cancer cells
GSE155757 NCOA6 is a potent prostate cancer suppressor essential for NFY-mediated restriction of EGFR overexpression

Data table header descriptions
ID_REF
VALUE log2 transformed, normalized signal intensity

Data table
ID_REF VALUE
A_21_P0014386 5.052321389
A_33_P3396872 5.116107967
A_33_P3267760 5.501656531
A_32_P194264 6.745598046
A_23_P153745 11.10363242
A_33_P3352837 5.095157577
A_21_P0011260 4.710493831
A_33_P3235816 4.965522328
A_21_P0014180 5.289809621
A_24_P944991 5.632830243
A_21_P0006507 4.87008485
A_23_P208706 11.24042138
A_33_P3388806 5.008174296
A_33_P3324839 5.177193326
A_24_P333494 8.881287827
A_22_P00006274 5.194533345
A_23_P161615 8.917914521
A_33_P3384958 5.308132444
A_22_P00018955 4.918592621
A_22_P00009547 5.177193326

Total number of rows: 52731

Table truncated, full table size 1322 Kbytes.




Supplementary file Size Download File type/resource
GSM4711609_mtb_JX_112256_AEG3H8v3_8064.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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