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#152108

T47D/TR-1 Cell Line

Cat. #152108

T47D/TR-1 Cell Line

Cat. #: 152108

Sub-type: Continuous

Unit size: 1x10^6 cells / vial

Availability: 8-10 weeks

Organism: Human

Tissue: Breast

Disease: Cancer

Model: Cancer 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: Anne Lykkesfeldt

Institute: Danish Cancer Society

Primary Citation: Kirkegaard et al. 2014. Cancer Lett. 344(1):90-100. PMID: 24513268.

Tool Details
Target Details
Applications
Handling
Related Tools
References
Documentation

Tool Details

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

  • Name: T47D/TR-1 Cell Line
  • Cancer: Breast cancer
  • Cancers detailed: Breast carcinoma;Tamoxifen resistant
  • Research fields: Cancer;Drug development
  • Tool sub type: Continuous
  • Parental cell: T47D/S2
  • Organism: Human
  • Tissue: Breast
  • Donor: Female, Caucasian, 54Y
  • Disease: Cancer
  • Growth properties: Adherent
  • Model: Cancer cell line
  • Conditional: Yes
  • Description: The T47D/TR-1 cell line is a tamoxifen-resistant derivative of the T47D human breast cancer cell line. It was developed by adapting T47D/S2 cells to 4-hydroxytamoxifen under reduced serum conditions to induce tamoxifen resistance. This adaptation results in a model that closely mimics the clinical progression of tamoxifen resistance in hormone receptor-positive breast cancer. T47D/TR-1 cells maintain estrogen receptor alpha (ERα) and progesterone receptor (PR) expression, characteristic of luminal A subtype breast cancer. They exhibit a polygonal epithelial morphology and are adherent in culture. The cell line serves as a valuable tool for investigating the molecular mechanisms underlying tamoxifen resistance, facilitating the identification of potential therapeutic targets and strategies to overcome resistance.
  • Application: Determining molecular mechanisms around tamoxifen resistance
  • Production details: Human breast cancer cell line derived from T47D/S2 cells by long-term culture in the presence of 4-hydroxytamoxifen under reduced serum conditions to induce tamoxifen resistance.
  • Biosafety level: 1
  • Cellosaurus id: CVCL_1D36

Target Details

  • Target: Oestrogen receptor

Applications

  • Application: Determining molecular mechanisms around tamoxifen resistance
  • Application notes: T47D/TR-1 cells are ER alpha positive and express progesterone receptor, although at reduced level compared to parental T7D/S2 cells. T47D/TR-1 are growth inhibited by fulvestrant.

Handling

  • Format: Frozen
  • Passage number: Passage 164 (AL3569, AL3570)
  • Growth medium: Phenol red free RPMI 1640 + 2% FCS + glutamax + 8ug Insulin/ml + 1 uM tamoxifen. Fetal Calf Serum (FCS) typically contains less estrogen than Fetal Bovine Serum (FBS) and is the preferred supplement for this cell line.
  • Temperature: 37° C
  • Atmosphere: 5% CO2
  • Unit size: 1x10^6 cells / vial
  • Shipping conditions: Dry ice
  • Storage medium: 10% DMSO in FCS
  • Storage conditions: Liquid Nitrogen
  • Subculture routine: Following thawing and counting, dilute the cell suspension with sufficient medium and distribute 5 mL each into T25 flasks to achieve a seeding density of 1.8 - 2.0 x 10^4 / cm2. Place in 37°C, 5% CO₂ incubator. Change medium after 24 hours to remove residual DMSO and then every 2-3 days. Subculture routine: Split 1:7 weekly (slow growing cell line) with Trypsin-EDTA for detachment at 37 °C for 5 minutes. Please also see detailed protocol within the Product Datasheet in the Documentation section below.
  • Mycoplasma free: Yes

Related Tools

  • Related tools: T47D/S2 Cell Line

References

  • Larsen et al. 2015. PLoS One. 10(2):e0118346. PMID: 25706943.
  • Larsen et al. 2015. BMC Cancer. 15(1):1-15. PMID: 25885472.
  • Thrane et al. 2014. Oncogene. 34(32):4199-4210. PMID: 25362855.
  • Kirkegaard et al. 2014. Cancer Lett. 344(1):90-100. PMID: 24513268.

Documentation

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