Journal: bioRxiv
Article Title: Selective Sensitivity of Ph-like B-ALL to BRG1 Inhibition Reveals a Novel Targeted Therapy Strategy
doi: 10.1101/2025.07.08.661805
Figure Lengend Snippet: A) Smarca4 expressions in different murine hardy B fractions – ‘CLP’: Common lymphoid progenitor, ‘Fr. A’: Pre-Pro B, ‘Fr. B’: Early Pro B, ‘Fr. C’: Late Pro B / Large Pre-B, ‘Fr. D’: Small Pre-B, ‘Fr. E’: Immature B, and ‘Fr. F’: Mature B cells (GSE38463). B) Expression of Smarca4 in different murine B developmental stages and lymphoma models (GSE26408). C) SMARCA4 expressions in B-ALL populations compared to T-ALL, CD19+, and CD34+ populations (GSE33315). D) SMARCA4 expressions in different subtypes of B-ALL populations (GSE11877). E) Western blot analysis of BRG1, BRM, and β-actin in four KMT2A -R (SEM, HB11;19, RS4;11, KOPN8) and two Ph-like (MUTZ5, MHH-CALL4) B-ALL cell lines. F) Mutational frequencies of different oncogenes in B-ALL patient populations from the COG study P9906 (GSE11877). G) Dependency analysis of SMARCA4 via the Cancer Dependency MAP website. Data are represented as individual values with mean ± SEM bars. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001 by One-way Anova Dunnett’s multiple comparison test.
Article Snippet: Human KMT2A -R (SEM, HB11;19, RS4;11, KOPN8) and Ph-like (MUTZ5, MHH-CALL4) B-ALL cell lines listed in Supplementary Table 2 , were obtained from the DSMZ biorepository (Braunschweig, Germany) validated by short tandem repeat (STR) analysis, and confirmed to be Mycoplasma-free every six months - .
Techniques: Expressing, Western Blot, Comparison