Figure 2
Figure 2. Role of CXCR4WHIM mutations in MYD88L265P-mutated WM. (A) PCA of the top 500 high variance genes within the WM patient samples using the first 2 principal components. WM patients with the MYD88L265PCXCR4WT genotype are shown in red; patients mutated for MYD88 with CXCR4 nonsense (NS) or frameshift (FS) mutations are shown in dark and light green, respectively; and patients with MYD88WTCXCR4WT are shown in purple. (B) Heat map of the 3103 genes differentially expressed between the MYD88L265PCXCR4WT and MYD88L265PCXCR4WHIM genotyped samples. Gene order was determined using hierarchical clustering of MYD88L265PCXCR4WT and MYD88L265PCXCR4WHIM expression data whereas the samples where arranged by genotype. Expression data for MYD88WTCXCR4WT WM and healthy donor B-cell samples were added to the heat map for comparison with intact clustered gene order. (C) Top predicted upstream targets of the differentially expressed genes from Ingenuity Pathway Analysis.

Role of CXCR4WHIM mutations in MYD88L265P-mutated WM. (A) PCA of the top 500 high variance genes within the WM patient samples using the first 2 principal components. WM patients with the MYD88L265PCXCR4WT genotype are shown in red; patients mutated for MYD88 with CXCR4 nonsense (NS) or frameshift (FS) mutations are shown in dark and light green, respectively; and patients with MYD88WTCXCR4WT are shown in purple. (B) Heat map of the 3103 genes differentially expressed between the MYD88L265PCXCR4WT and MYD88L265PCXCR4WHIM genotyped samples. Gene order was determined using hierarchical clustering of MYD88L265PCXCR4WT and MYD88L265PCXCR4WHIM expression data whereas the samples where arranged by genotype. Expression data for MYD88WTCXCR4WT WM and healthy donor B-cell samples were added to the heat map for comparison with intact clustered gene order. (C) Top predicted upstream targets of the differentially expressed genes from Ingenuity Pathway Analysis.

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