Cat. #153600
KPC Cell Line (mixed genetic background)
Cat. #: 153600
Sub-type: Continuous
Unit size: 1x10^6 cells / vial
Availability: 3-5 days
Organism: Mouse
Disease: Cancer
Model: Transgenic
£575.00
This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.
Contributor
Inventor: Jennifer Morton
Institute: Cancer Research UK, Glasgow Beatson Institute
Tool Details
*FOR RESEARCH USE ONLY
- Name: KPC Cell Line (mixed genetic background)
- Alternate name: PDAC cell line
- Tool sub type: Continuous
- Organism: Mouse
- Disease: Cancer
- Model: Transgenic
- Conditional: No
- Description: The KPC mouse is an established and clinically relevant model of pancreatic ductal adenocarcinoma (PDA) which develops many key features observed in human PDA including pancreatic intraepithelial neoplasia alongside a robust inflammatory reaction including exclusion of effector T cells. Metastases are observed in around 80% of KPC animals located primarily in the liver and lungs. Mutations in both KRAS and TP53genes are found in around 80% and 70% of all human PDAs respectively. Tumours present in KPC mice display many immuno-histological markers of PDA as well as possessing complex genomic rearrangements a key sign of genomic instability. The co-morbidities, cachexia, jaundice and ascites, associated with human PDA are also observed in this model and most pancreatic tumours are resistant to chemotherapy. The KPC mouse contains a conditional point mutation in the transformation related protein 53 gene (TP53R172H), and a point mutation in the KRAS gene (KRASG12D) both of which generate non-functional proteins. A lox-stop-lox termination sequence is encoded upstream of both mutated genes to prevent expression in the absence of Cre recombinase. PDX1 (pancreatic and duodenal homeobox 1) is a transcription factor necessary for pancreatic development. The PDX1 promoter enables expression of Cre recombinase in acini, islet and duct cells of the pancreas. Cre-mediated recombination excises the two lox-stop-lox termination sequences and enables expression of both oncogenes: KRASG12D and TP53R172H in pancreatic tissue. Tissues not expressing Cre recombinase remain functionally heterozygous of the KRAS and TRP53 loci.
- Biosafety level: 1
- Additional notes: These cells are from mice with a mixed genetic background KPC Subtype: C57Bl6/J
Target Details
- Target: TP53, KRAS
Applications
- Application notes: These cells are from mice with a mixed genetic background KPC Subtype: C57Bl6/J
Handling
- Format: Frozen
- Growth medium: They all grow in DMEM (+10% FCS, 1% L-Glut and 1% Pen/strep). They may take a wee bit of time coming back up, don't panic, just be gentle with them.
- Unit size: 1x10^6 cells / vial
- Shipping conditions: Dry ice
- Storage conditions: Liquid Nitrogen
- Mycoplasma free: Yes
Related Tools
- Related tools: KPC Cell Line (C57/BL6 genetic background)
References
- Li et al. 2014. Gastroenterology. 146(5):1386-96.e1-17. PMID: 24462734.
- Fascin is regulated by slug, promotes progression of pancreatic cancer in mice, and is associated with patient outcomes.
- Hingorani et al. 2005. Cancer Cell. 7(5):469-83. PMID: 15894267.
- Trp53R172H and KrasG12D cooperate to promote chromosomal instability and widely metastatic pancreatic ductal adenocarcinoma in mice.