#153600

KPC Cell Line (mixed genetic background)

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
Target Details
Applications
Handling
Related Tools
References

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.