fR5 Cell Line

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. 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.

Contributors

Inventor Institute
Joyce Taylor-Papadimitriou ; Sidney Chang Cancer Research UK, Lincoln's Inn Fields Institute
Cat. #: 153247
Unit size: 1×10^6 cells / vial
Cancer types: Breast cancer
Research Fields: Cancer;Drug development
Organism: Human
Tissue: Breast
Gender: Female
Model: Immortalised Line
Growth properties: Adherent
Cancer Types In Detail: Breast cancer
Primary citation: Chang et al. 1982. Cancer Res. 42(5):2040-2053. PMID: 6279290.
Product 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.
Gender: Female
Conditional: No
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
Disease: Cancer
Format: Frozen
Shipping conditions: Dry ice
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
References:

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

Images

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fR5 Cell Line. Image courtesy of the European Collection of Authenticated Cell Cultures (ECACC)

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