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Journal: Genome Medicine
Article Title: Utilizing genomics to identify novel immunotherapeutic targets in multiple myeloma high-risk subgroups
doi: 10.1186/s13073-025-01503-y
Figure Lengend Snippet: Characteristics of candidate targets identified in ND and RR populations from two independent datasets. A General workflow of the target identification process. B A heatmap demonstrating all identified candidate genes in ND and RR population from MMRF and IU datasets with various annotations. C Expression level of selected genes. D Ranked expression of 5,092 proteins documented in Anderson et al. . Numbers after gene names: rank. E A radar plot summarizing key characteristics among LAX1 , ITGA4 , and TNFRSF17 /BCMA. Range (from center to edge): toxicity (healthy organs): 2~0; toxicity (blood cells): 0~1845; protein exp: 24.8~37221.6; essentiality: 0~ −1.75; hazard ratio (PFS): 1~1.28; mRNA exp: 3~7.6. Range in toxicity, protein expression, essentiality, hazard ratio, and mRNA exp indicated lowest to highest among 98 candidate genes. F Log 2 -scaled median fluorescence intensity (MFI) of TNFRSF17/BCMA and ITGA4/CD49d detected by flow cytometry in 15 MM cell lines. G Density plots indicating MFI (blue peaks) of ITGA4 /CD49d compared to the isotype control (grey peaks) across 6 MM cell lines. Log 2 MFI: Log 2 -scaled MFI. Highlighted genes in B : well-established targets or novel targets found in this study and validated by flow cytometry
Article Snippet: For the direct immunostaining, cells were labeled with PE anti-human BCMA (Biolegend),
Techniques: Drug discovery, Expressing, Fluorescence, Flow Cytometry, Control