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Contributor Information

  • Name Joyce Taylor-Papadimitriou ; Sidney Chang
  • Institute Cancer Research UK, Lincoln's Inn Fields Institute
  • Primary citation Chang et al. 1982. Cancer Res. 42(5):2040-2053. PMID: 6279290.

Tool Details

  • Tool name: fR5 Cell Line
  • Tool type: Cell Lines
  • Organism: Human
  • Tissue: Breast
  • Gender: Female
  • Cancer type: Breast cancer
  • Disease: Cancer
  • Growth properties: Adherent
  • Model: Immortalised Line
  • Conditional: No
  • Application: Investigating relationship between transformation and differentiation
  • Description: The fR5 Cell Line was established by infecting milk cultures with with simian vacuolating virus 40 (SV40). fR5 cells do not express Muc-1 (also known as HMFG-1 antigen) which is a mucin-like component of human milk fat globule membranes.

    fR5 cells display anchorage independent growth in soft agar and are positive for SV40 T-antigen. Early passages were non-tumourigenic in nude mice.

    They are negative for keratins 4, 6, 7, 8, 10, 13 14, 16, 17, 18 and 19. Although fR5 is morphologically different from fR2, they have probably been derived from a common precursor cell since the karyotypes are similar. Karyotype analysis revealed hypotetraploidy and several rearrangements involving chromosome 1 and 11 which are frequently found in breast carcinomas and lines derived from metastatic pleural effusions.

    This cell line could be useful for studying the relationship between transformation and differentiation in human mammary epithelial cells.
  • Research area: Cancer; Drug development
  • Production details: The breast epithelial cell line fR5 was established in 1982 by infecting suspensions of primary milk cultures with wild-type SV40.
  • Cellosaurus ID: CVCL_2445

  • For Research Use Only

Target Details

Application Details

  • Application: Investigating relationship between transformation and differentiation

Handling

  • Format: Frozen
  • Growth medium: Split sub-confluent cultures (70-80%) 1:10 i.e. seeding 1 x 10,000 cells / cm2 using 0.25% trypsin or trypsin/EDTA; 5% CO2; 37° C.

    Culture Medium: RPMI 1640 + 2mM Glutamine + 10ug/ml insulin + 5ug/ml hydrocortisone + 10% FBS
  • Shipping conditions: Dry ice

Documentation

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References

  • •  Chang et al. 1982. Cancer Res. 42(5):2040-2053. PMID: 6279290.