PDX Breast Cancer Model WHIM26

Technical Information
WHIM26 is a highly characterized, HER2-, ER+, PR+ breast cancer PDX model. Derived from a nodal metastasis, this model is whole genome sequenced.

Technical Data

Whole Genome Sequenced
Yes
RNA Sequence
No

Tumor Information

Availability
Available
Tumor Site
Metastasis: Node
Patient Number
26

Patient Demographics

Age at Diagnosis
59
Patient Race
Caucasian
Family History
None

PAM50 Subtype

PAM50 Originating Tumor
Luminal B
PAM50 Early Passage
Luminal A
PAM50 Late Passage
Luminal B

Genotype/Mutations

ER Status
Positive
PR Status
Positive
HER2 Status
Negative
p53 Genotype
WT
PIK3CA Genotype
WT
ESR1 Genotype
WT
Phosphoprotein Highest Rank
mTOR_pS2448

Pathology

Specimen Type
Surgical specimen -- lymph node, right supraclavicular, biopsy
Clinical Stage, Diagnosis
N/A
Pathological Stage
2A
Sample Stage
4
Pathology
Metastatic micropapillary carcinoma
Tumor Grade
N/A
Metastatic Site List
Right lower lobe lung mass; Skin (Chest wall); Bone; Bladder; Supraclavicular lymph node
Systemic Treatments
Premarin; Anastrozole; Estradiol; Arimidex; Estradiol, Tamoxifen; Grafted sample for WHIM26; Xeloda, Radiation to chest wall and right supraclavicular fossa
Overall Survival (months)
283

PAM50 Subtype Expression

PAM50 Subtype Microarray
PDX Breast Cancer Model WHIM26 - PAM50 Subtype Microarray
Microarray showing PAM50 subtype. Unsupervised hierarchical clustering of samples using all genes of the microarrays except the stromal-related genes. 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, lumenal A; light blue, lumenal B; yellow, Claudin-low. Below the array tree and the subtype identification row, the heatmap of the 50 PAM50 genes as well as selected tight-junction-related genes (E-cadherin [CDH1], claudin 3 [CLDN3], CLDN4, and CLDN7) are shown. The stromal-related genes were identified after a two-class paired SAM was performed with an FDR of 0% between 18 paired progenitor human tumors and xenografts.
PAM50 Microarray Validation
PDX Breast Cancer Model WHIM26 - PAM50 Microarray Validation
Validation of PAM50 microarray. Coclustering of 250 human breast samples representing all the PAM50 intrinsic subtypes and 22 HIM models using the 50 PAM50 genes. Gene expression data of all samples has been obtained using 244K Agilent microarrays.
Claudin Low Signature
PDX Breast Cancer Model WHIM26 - Claudin Low Signature
Microarray of 807 genes that make up the Claudin-low signature. On the right, the expression of each gene (up- or downregulated) of the Claudin-low signature is shown. The two Claudin-low samples (WHIM 12 and WHIM 17) are identified below the array tree.

ER, HER2 and PR Expression

ER and HER2 Western Blots
PDX Breast Cancer Model WHIM26 - ER and HER2 Western Blots
ER and HER2 protein expression. Tumor lysates from ER-positive (A) and ER-negative (B) WHIM lines were analyzed by western blot to confirm ER and HER2 status. Lysates from ER-negative WHIM lines were also probed with antibodies against the cytokeratin 5/6 (CK 5/6) and CD44 markers. The MCF7 (ER-positive), SKBR3 (ER-negative, HER2-positive) and MDA-MB-231 (ER-negative, CD44-positive) breast cancer cell lines were included as blotting controls.

Circos Plots & Phosphoprotein Expression

Phosphoprotein Expression
PDX Breast Cancer Model WHIM26 - Phosphoprotein Expression
Phosphoprotein expression by RPPA. The RPPA data for WHIM samples and 386 TCGA samples were combined after standardizing the data for each marker (i.e., subtracting the mean and then divided by the standard deviation) in the separate data sets. The combined samples were hierarchically clustered using a Pearson correlation based distance matrix ((1-rho)/2, where rho is the Pearson correlation matrix) and the “ward” linkage based on Ward’s minimum variance. In every case the samples from each WHIM line clustered adjacently, including the two double PDX model isolations (WHIM2 and WHIM5, WHIM20 and WHIM23). This demonstrates that intra-PDX heterogeneity was considerably less than the inter-tumoral heterogeneity in a large RPPA data set and was relatively stable over time and passage.
Protocols & Documents
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