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Series GSE74377 Query DataSets for GSE74377
Status Public on Oct 26, 2016
Title Overexpression of PHF8 promotes an EMT-related gene signature in MCF10A cells
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary PHF8 exerts distinct functions in different types of cancer. However, the mechanisms underlying its specific functions in each case remain obscure. To establish whether overexpression of PHF8 regulates the TGF-β induced the epithelial-mesenchymal transition (EMT), we treated MCF10A-Mock (control) and MCF10A-PHF8wt (overexpressing wild-type PHF8) cells with TGF-β1 for 0, 24, 48 and 72 hours and performed RNA-seq in biological duplicates. Our data indicated that EMT gene signatures were significantly enriched in MCF10A-PHF8 cells with TGF-β1 treatment at all time points, strongly indicating that PHF8 overexpression induces a sustained EMT signaling program.
 
Overall design mRNA profiles of MCF10A-Mock (control) and MCF10A-PHF8 with TGF-β1 treatment for 0, 24, 48 and 72 hours were generated by RNA-seq, in duplicate, using HiSeq2500 instrument.
 
Contributor(s) Shao P, Qi HH
Citation(s) 27899639
Submission date Oct 27, 2015
Last update date May 15, 2019
Contact name Noah S Butler
E-mail(s) noah-butler@uiowa.edu
Organization name University of Iowa
Department Department of Microbiology and Immunology
Lab Butler Lab
Street address 4-350 BSB, 51 Newton Road
City Iowa City
State/province IA
ZIP/Postal code 52242
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (16)
GSM1919088 MCF10A/Mock-NC rep1
GSM1919089 MCF10A/Mock-TGFβ1-24hr rep1
GSM1919090 MCF10A/Mock-TGFβ1-48hr rep1
Relations
BioProject PRJNA299891
SRA SRP065305

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE74377_RNAseq_DESeq2.xlsx.gz 6.8 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Processed data are available on Series record
Raw data are available in SRA

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