Coming soon HCI-026 PDX

Tool Details

*FOR RESEARCH USE ONLY

• Research area: Breast Cancer
• Description: Please register your interest through the enquiry button (quote not currently available)
  
  Human breast cancer-derived xenograft that retains high fidelity to original tumour and provides valuable resources for drug discovery and precision oncology. This panel of Patient Derived Xenografts provide models for some of the deadliest forms of breast cancer including drug-resistant, metastatic tumours, and endocrine-resistant estrogen receptor-positive (ER+) and HER2+ tumours.
  
  Sample collected in 2016 from spine metastasis of female, age 55 at time of collection with a primary diagnosis of IDC; 2013. Patient had no prior history of smoking, and had clinical metastasis detected in bone and liver. Patient had undergone radiation therapy of breast in 2013, and received systemic treatment of cyclophosphamide, paclitaxel 2014; tamoxifen 2014-2016 prior to sample collection. Patient characteristics were as follows - ER status: positive, PR status: positive (3%), HER2 status: negative. PDX characteristics were as follows - ER status: positive, PR status: negative, HER2 status: negative. PDX information: PAM50 subtype is luminal B and metastasis in lung detected.

Patient Details

• Cancer type: Breast Cancer
• Cancer subtype: Infiltrating Ductal Carcinoma
• Biopsy site: Spine metastasis
• Gender: Female
• Patient ethnicity: not disclosed
• Treatment history: Pretreated: Patient had undergone radiation therapy of breast in 2013, and received systemic treatment of cyclophosphamide, paclitaxel 2014; tamoxifen 2014-2016 prior to sample collection

Engraftment Details

• Mice passaged: Yes
• Engraftment site: Cleared mammary fat pad
• Host strain: Immunocompromised mice NOD scid gamma (NSG) Jackson Laboratory 5557; NOD/scid, Jackson Laboratory 1303 or NOD rag gamma (NRG), Jackson Laboratory 7799
• Histology: PAM50 subtype Luminal B
• Production details: Fresh or thawed human breast tumour fragments were implanted into the cleared inguinal mammary fat pad of female Immune-compromised mice. For bone metastasis samples, bone fragments were coimplanted. For liquid specimens, pleural effusion, or ascites fluid, 1-2 milion cells were injected into cleared mammary fat pads in Matrigel. For ER+ tumours, mice were dosed with E2 beeswax pellets and given supplemental E2 via drinking water. When tumours reached 1-2 cm in diameter, tumours were aseptically collected and reimplanted into new m ice or banked. Estrogen-independent ER+ breast PDX models were generated when ER+ PDX tumours were transplated into overiectomized mice without E2 supplementation.

Handling

• Additional notes: Additional Information on PDX establishment: https://www.nature.com/articles/s43018-022-00337-6/figures/9

References

• Tufail, et al. 2024. Journal of Translational Med. Jan 3:22(1):15. PMID: 38172946
• Bhattacharya, et al. 2023. Journal of Experimental & Clinical Cancer Research. Dec 16:42(1):343. PMID: 38102637
• Prekovic, et al. 2023. EMBO Molecular Medicine. Dec 7:15(12):e17737. PMID: 37902007
• Daneshdoust, et al. 2023. Cells. Sep 30:12(19):2338. PMID: 37830602
• Wang, et al. 2023. Cell Bioscience. Dec 1:13(1):224. PMID: 38041134
• Guillen, et al. 2022. Nature Cancer. Feb 3(2):232-250. PMID: 35221346