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Series GSE94393 Query DataSets for GSE94393
Status Public on Aug 02, 2017
Title Expression data from KEAP1 overexpression and NRF2 siRNA knockdown of A549 NSCLC cell
Organism Homo sapiens
Experiment type Expression profiling by array
Summary KEAP1 overexpressed and NRF2 siRNA knockdown A549 NSCLC cells were used to identify downstream genes of NRF2 pathway separately and by combinatorial analysis. We used triplicate microarrays of transfected A549 cells with mKeap1-GFP for overexpression, siRNAs targeting NRF2 for knockdown and siGFP as control respectively. As a result, we identified several genes which are involved in cancer metabolic functions in these cells.
We used microarrays to identify the gene downregulated in both KEAP1 overexpressed and NRF2 siRNA knockdown A549 NSCLC cells and found a subset of downregulated genes which are involved in metabolic functions.
 
Overall design We divided microarrays into three groups. One group with A549 cells that were stably transfected with mKeap1-GFP construct for overexpression, second group with knockdown of NRF2 with specific siRNA and third group contains siGFP transfected control cells. Triplicates of both KEAP1 overexpression and NRF2 siRNA knockdown groups were analyzed and compared with control microarray data.
 
Contributor(s) Namani A, Wang XJ, Tang X
Citation(s) 29050246
Submission date Feb 01, 2017
Last update date Aug 23, 2018
Contact name XIUWEN TANG
E-mail(s) xiuwentang@zju.edu.cn
Organization name ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE
Department BIOCHEMISTRY AND GENETICS
Street address YUHANGTONG ROAD
City HANGZHOU
ZIP/Postal code 310000
Country China
 
Platforms (1)
GPL15207 [PrimeView] Affymetrix Human Gene Expression Array
Samples (9)
GSM2474572 KEAP1 overexpression biological rep1
GSM2474573 KEAP1 overexpression biological rep2
GSM2474574 KEAP1 overexpression biological rep3
Relations
BioProject PRJNA369558

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Supplementary file Size Download File type/resource
GSE94393_RAW.tar 15.7 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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