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Status |
Public on Aug 06, 2013 |
Title |
FGFR2 Signaling Underlies p63 Oncogenic Function in Squamous Cell Carcinoma |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
This study was designed to examine the requirement for the p63 transcription factor in Squamous Cell Carcinoma (SCC) tumor maintenance in an in vivo murine system. A tamoxifen-inducible Keratin 14-driven Cre recombinase transgene was used to conditionally excise p63 in advanced murine SCC tumors. These data show the context-dependent regulation of p63 target genes in cancer.
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Overall design |
Total RNA from murine Squamous Cell Carcinoma tumors was examined 1-3 days following genomic excision of TP63 in Keratin 14-expressing tumor cells.
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Contributor(s) |
Ramsey MR, Ellisen LW |
Citation(s) |
23867503 |
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Submission date |
Apr 10, 2013 |
Last update date |
Jan 16, 2019 |
Contact name |
Matthew Ramsey |
Organization name |
Brigham and Women's Hospital
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Department |
Dermatology
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Lab |
Matthew R. Ramsey
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Street address |
77 Ave Louis Pasteur, HIM 668
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02115 |
Country |
USA |
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Platforms (1) |
GPL6887 |
Illumina MouseWG-6 v2.0 expression beadchip |
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Samples (6)
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Relations |
BioProject |
PRJNA196677 |