HCI-013-EI breast cancer PDX

HCI-013-EI PDX: Human breast cancer-derived xenograft retains high fidelity to original tumour. Valuable resource for drug discovery and precision oncology.

Contributors

Inventor Institute
Alana L Welm, Yi-Chun Lin, Yoko Sakata DeRose The University of Utah Research Foundation
Cat. #: 162082
Gender: Female
Biopsy Site: Pleural Effusion Fluid
Patient ethnicity: Caucasian
Treatment History: Pretreated: Patient had undergone radiation therapy to bone other than spine (2007) and spine (2010) and had systemic treatment of leuprolide 2003-2008; letrozole 2003-2007; zolendronic acid 2003-2010; tamoxifen 2007-2008; exemestane 2008; cyclophosphamide, 2008; 5-fluorouracil, methotrexate 2008; capecitabine 2008-2009; paclitaxel 2009; nab-paclitaxel 2009; doxorubicin 2009-2010; carboplatin, gemcitabine 2010 prior to sample collection
Primary citation: Guillen, et al. 2022. Nature Cancer. Feb; 3(2):232-250. PMID: 35221336
Product description: Human breast cancer patient-derived xenograft (PDX) model that retains high fidelity to original tumour, including spatial structure, intratumour heterogeneity, genomic features, tumour growth rate, metastatic patterns, and drug responses. These highly translatable PDX models can be used to more accurately assess therapeutic efficacy and predict patient responses in preclinical drug validation studies than traditional models. This panel of PDX models includes some of the deadliest forms of breast cancer such as drug-resistant, metastatic tumours, and endocrine-resistant estrogen receptor-positive (ER+) and human epidermal growth factor receptor positive (HER2+) tumours. Sample collected in 2010 from pleural effusion of Caucasian female, age 53 at time of collection with a primary diagnosis of ILC; 2003. Patient had no prior history of smoking, and experienced clinical metastasis to the lung, liver and pericardium. Patient had undergone radiation therapy to bone other than spine (2007) and spine (2010) and had systemic treatment of leuprolide 2003-2008; letrozole 2003-2007; zolendronic acid 2003-2010; tamoxifen 2007-2008; exemestane 2008; cyclophosphamide, 2008; 5- fluorouracil, methotrexate 2008; capecitabine 2008-2009; paclitaxel 2009; nab-paclitaxel 2009; doxorubicin 2009-2010; carboplatin, gemcitabine 2010 prior to sample collection. Patient and PDX characteristics were as follows – ER status: positive, PR status: positive, HER2 status: negative. PDX information: generated from HCI-013 two years later and grown in ovx mice, PAM50 subtype is luminal B, not estrogen dependent, PTEN positive by IHC, and shows metastasis to lung.
Initial handling information: Implant into the cleared inguinal mammary fat pad of female Immune-compromised mice (NOD.SCID). Time to grow to 2cm: 1-2 months. Positive ER status
Additional notes: Additional Information on PDX establishment: https://www.nature.com/articles/s43018-022-00337-6/figures/9
Mice Passaged: Yes
Engraftment Site: Cleared mammary fat pad
Sample Type: HCI-013 PDX Tissue Fragment
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.
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: 35221336

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