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Get Free AccessFigure S1. Inhibition of Axl by shRNA. Figure S2. Assessment of half maximal inhibitory concentration (IC50) for BGB324 in human CD34+ cells from healthy donors. Figure S3. Treatment with BGB324 increased apoptosis and decreased proliferation of CML cell lines. Figure S4. Reduction of BCR-ABL and Crkl phosphorylation by imatinib. Figure S5. Treatment with imatinib and BGB324 does not induce an additive inhibitory effect on phosphorylation of Erk and Akt. Figure S6. BCR-ABL and Crkl phosphorylation are not affected by imatinib or BGB324 in KCL-22 T315I mutated cells. Figure S7. Colony forming assay using primary CD34+ cells isolated from healthy donors treated for 72 h with 1, 3 or 5 μM of BGB324 (n=2). Figure S8. BGB324 increases apoptosis of primary CML cells.
Isabel Ben‐Batalla, Robert G. Erdmann, Heather G. Jørgensen, Rebecca Mitchell, Thomas Ernst, Gunhild von Amsberg, Philippe Schafhausen, Janna L. Velthaus, Stephen E. Rankin, Richard E. Clark, Steffen Koschmieder, Alexander Schultze, Subir K. Mitra, Peter Vandenberghe, Tim H. Brümmendorf, Peter Carmeliet, Andreas Hochhaus, Klaus Pantel, Carsten Bokemeyer, G. Vignir Helgason, Tessa L. Holyoake, Sonja Loges (2023). Revised supplemental figures from Axl Blockade by BGB324 Inhibits BCR-ABL Tyrosine Kinase Inhibitor–Sensitive and -Resistant Chronic Myeloid Leukemia. , DOI: https://doi.org/10.1158/1078-0432.22462538.v1.
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Type
Preprint
Year
2023
Authors
22
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1158/1078-0432.22462538.v1
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