#160436

UM-UC-1 (Human bladder transitional cell carcinoma) cell line

Cat. #160436

UM-UC-1 (Human bladder transitional cell carcinoma) cell line

Cat. #: 160436

Unit size: 1x10^6 cells / vial

Organism: Human

Tissue: Lymphatic Tissue

Disease: Cancer

Model: Tumourigenic cell line

£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: H. Grossman ; Anita Sabichi

Institute: University of Michigan

Tool Details
Handling
Related Tools
References

Tool Details

*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)

  • Name: UM-UC-1 (Human bladder transitional cell carcinoma) cell line
  • Alternate name: UM-UC-1; UMUC1; University of Michigan-Urothelial Carcinoma-1
  • Cancer type filter: Bladder cancer
  • Cancers detailed: Human bladder translational cell carcinoma
  • Research fields: Cancer
  • Organism: Human
  • Tissue: Lymphatic Tissue
  • Disease: Cancer
  • Growth properties: Adherent
  • Model: Tumourigenic cell line
  • Description: UM-UC-1 is a well-characterised human urothelial carcinoma cell line derived from lymphatic metastases of grade II transitional cell carcinoma from a 26-year old male patient. This tumorigenic cell line demonstrates rapid tumour formation in nude mice (1-1.5cm diameter in <3 weeks) and exhibits strong p53 nuclear overexpression by IHC analysis. This cell line has a high level of coxsackie adenovirus receptor. UM-UC-1 was more resistant to adenoviral gene transduction than several of the other cells evaluated. UM-UC-1 is part of the comprehensive 11 cell UM-UC panel deposited by the university of Michigan

Handling

  • Format: Frozen
  • Growth medium: Cells were grown in MEM + 1% NEAA + 2mM Glutamine + 10% Foetal Bovine Serum (FBS).
  • Unit size: 1x10^6 cells / vial
  • Shipping conditions: Dry ice
  • Subculture routine: Split sub confluent cultures (70-80%) 1:4 to 1:10 i.e. seeding at 2-4x10,000 cells/cm2; using 0.05% trypsin or trypsin/EDTA; 5% CO2, 37°C. Doubling time approximately 26 hours.

Related Tools

  • Related tools: UM-UC-4 (Human adenocarcinoma lymph node metastasis) cell line ; UM-UC-3 (Human bladder transitional cell carcinoma) cell line ; UM-UC-5 (Human squamous cell carcinoma of the bladder) cell line ; UM-UC-7 (Human transitional cell carcinoma of the bladder) cell line ; UM-UC-9 (Human transitional cell carcinoma of the bladder) cell line ; UM-UC-10 (Human transitional cell carcinoma of the bladder) cell line ; UM-UC-11 (Human transitional cell carcinoma of the bladder) cell line ; UM-UC-13 (Human...

References

  • Grossman et al. 1984. J Urol. 132(4):834-7. PMID: 6471236.
  • Grossman et al. 1986. J Urol. 136(5):953-9. PMID: 3761468.
  • Sabichi et al. 2006. J Urol. 175(3 Pt 1):1133-7. PMID: 16469639.
  • Park et al. 2008. J Natl Cancer Inst. 100(19):1401-11. PMID: 18812553.
  • Chiong et al. 2009. J Urol. 181(6):2737-45. PMID: 19375735.
  • Barretina et al. 2012. Nature. 483(7391):603-7. PMID: 22460905. Guo et al. 2013. J Pathol. 230(1):17-27. PMID: 23401075.
  • Klijn et al. 2015. Nat Biotechnol. 33(3):306-12. PMID: 25485619.
  • Yu et al. 2015. Nature. 520(7547):307-11. PMID: 25877200.
  • Earl et al. 2015. BMC Genomics. 16:403. PMID: 25997541.
  • Scholtalbers et al. 2015. Genome Med. 7:118. PMID: 26589293.
  • Nickerson et al. 2017. Oncogene. 36(1):35-46. PMID: 27270441.
  • Zuiverloon et al. 2018. Bladder Cancer. 4(2):169-83. PMID: 29732388.
  • Dutil et al. 2019. Cancer Res. 79(6):1263-73. PMID: 30894373.
  • Ghandi et al. 2019. Nature. 569(7757):503-8. PMID: 31068700.

Tool enquiry

Please ensure you use your organisation email address rather than personal where possible, as this helps us locate your organisation in our system faster.

Please note we may take up to three days to respond to your enquiry.

CancerTools.org uses the contact information provided to respond to you about our research tools and service. For more information please review our privacy policy.