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Status |
Public on Jul 06, 2023 |
Title |
p53 inhibitor iASPP is an unexpected suppressor of KRAS and inflammation driven pancreatic cancer |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
To investigate the transcriptomic effects of iASPP deletion or p53 mutation in the KRASG12D background Pdx1-Cre was used to delete iASPP in oncogenic KRASG12D expressing (KC) background to generate KC;iASPPΔ8/Δ8 mice. KC and KC;iASPPΔ8/Δ8 mice were then crossed with mice containing a p53R172H allele (equivalent to human p53 hotspot mutation R175H) to generate KPC and KPC;iASPPΔ8/Δ8 cohorts. Primary cell cultures were then derived from pancreatic ductal adenocarcinoma tissue for RNA-seq.
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Overall design |
Comparative gene expression profiling analysis of RNA-seq data for KC, KC;iASPPΔ8/Δ8,KC, and KC;iASPPΔ8/Δ8 mouse cell lines.
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Contributor(s) |
Miller P, Owen R, Amess R, Lu X |
Citation(s) |
37270580 |
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Submission date |
Mar 03, 2023 |
Last update date |
Jul 06, 2023 |
Contact name |
Xin Lu |
E-mail(s) |
xin.lu@ludwig.ox.ac.uk
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Phone |
+44 1865 617507
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Organization name |
University of Oxford
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Department |
Ludwig Institute for Cancer Research
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Street address |
Old Road Campus
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City |
Oxford |
State/province |
Oxfordshire |
ZIP/Postal code |
OX3 7DQ |
Country |
United Kingdom |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (16)
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Relations |
BioProject |
PRJNA940781 |