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. 2018 Feb 5;37(17):2237–2250. doi: 10.1038/s41388-017-0079-x

Fig. 3.

Fig. 3

Ibrutinib inhibits cell growth in ERBB4High/BTKLow cell lines. a Cell proliferation assays were performed in ERBB4High/BTKLow and ERBB4Low/BTKLow cell lines after ibrutinib treatment (6 days, 1 μM). The number of viable cells is reported as a percentage of the respective control (DMSO treated). b Dose-response curves after ibrutinib treatment (6 days, 1 nM–10 μM). c Protein levels of ERBB4 and downstream proteins (MEK, ERK, and AKT) in ibrutinib-treated H661 cells (0.1–1 μM). d Western blots for ERBB4 and GAPDH in cell lines infected with GFP or shRNA against ERBB4 or scramble. e Protein levels of EGFR and ERBB2 after shRNA infection. f Cell proliferation assay for cells infected with shERBB4, scramble or GFP. g Tumor growth of H661 cell-derived mouse xenografts (n = 10) after daily treatment of ibrutinib (5 mg/kg) and buffer only control for 60 days. The P-value calculated by the two-tailed T-test is shown, and the two-tailed Mann–Whitney U-test P-value was 0.01. (**P < 0.002; ***P < 0.001; ****P < 0.0001)