Bringing clarity to your research, Horizon is excited to exclusively offer the largest collection of highly characterized, deeply sequenced patient-derived xenograft (PDX) models of breast cancer available today. The WHIM (Washington University Human-in-Mouse) collection was developed by Shunqiang Li & Matthew Ellis at Washington University as published in Cell Reports.
This breast cancer PDX collection has undergone whole genome sequencing (WGS), with care to remove contaminating mouse signal. Additionally, WGS has been performed on the originating tumors, early and late passages of PDX, demonstrating striking similarity and faithful modeling of the original tumor. These PDX models are implanted as dissociated cells into immunodeficient mouse models which may then be used for in vivo efficacy studies.
Horizon offers this collection as ungrafted PDX heterogeneous cell suspensions for use in your facility. Additionally, Horizon offers a number of services around the WHIM breast cancer PDX collection, including in vivo efficacy studies and ex vivo proliferation studies. For services, consult with our team of expert scientists to design your study, provide us with your test articles, and then our team of highly trained staff will demonstrate the effect of your test article on PDX grown in immunodeficient mice.
This collection comprises a broad range of breast cancer PDX models, including ER+ models, triple-negative models, and HER2+ models. This allows the study of different types of human breast cancer tumors in an in vivo model system, and represents a key tool in the development of personalized medicines. These models accurately model real patient tumors, enabling researchers to discover important genetic differences, develop biomarkers to distinguish these variations, and ultimately develop patient-specific therapies.
The colors of the array tree and the squares below the tree denote the subtype call of each sample. Red, basal-like; pink, HER2-enriched; dark blue, luminal A; light blue, luminal B; yellow, Claudin-low.
Figure 1. Microarray showing PAM50 subtype.