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Status |
Public on Feb 09, 2017 |
Title |
DLX3 alters transcriptomic profile of adhesion, cell cycle, and cell death in Squamous Cell Carcinoma Cells |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Reinstatement of DLX3 into SCC13 cells upregulates genes involved with cell cycle exit, signaling, and adhesion whiles downregulates genes involved with cell death, proliferation, and movement.
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Overall design |
We used RNA-sequencing data analysis to assess gene expression in SCC13 cells infected with Adeno-GFP or Adeno-DLX3 in order to understand the effects of DLX3 in a Squamous Cell Carcinoma Cell Line. We identified a specific subset of genes involved in regulation of cell cycle arrest and inhibition of apoptosis.
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Contributor(s) |
Palazzo E, Kellett MD, Cataisson C, Gormley A, Bible PW, Pietroni V, Radoja N, Hwang J, Blumemberg M, Yuspa SH, Morasso M |
Citation(s) |
26522723 |
Submission date |
Apr 09, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Hong-wei Sun |
Organization name |
NIAMS
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Department |
Office of Science & Technology
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Lab |
Biodata Mining & Discovery Section
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Street address |
9000 Rockville Pile
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL16791 |
Illumina HiSeq 2500 (Homo sapiens) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE67714 |
DLX3-dependent p53 signaling network controls keratinocyte cell cycle and squamous tumor growth |
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Relations |
BioProject |
PRJNA280746 |
SRA |
SRP057020 |