Additional file 3: of A kinase inhibitor screen identifies a dual cdc7/CDK9 inhibitor to sensitise triple-negative breast cancer to EGFR-targeted therapy
journal contributionposted on 01.07.2019 by Ronan McLaughlin, Jichao He, Vera Noord, Jevin Redel, John Foekens, John Martens, Marcel Smid, Yinghui Zhang, Bob Water
Any type of content formally published in an academic journal, usually following a peer-review process.
Figure S1. Resistance of TNBC cells to EGFR-TKIs. a. Effect of lapatinib on induction of apoptosis in selected lapatinib-resistant and lapatinib-sensitive TNBC cell lines. Hs578T, BT549, SKBR7 and HCC1806 cells were treated with lapatinib (3.16 μM) as indicated, for 24 h, 48 h or 72 h, respectively, stained with Annexin-V and Hoechst, followed by imaging and image quantification. Relative cell death was quantified by normalising the intensity of Annexin-V signal to that of DMSO control. One-way ANOVA **** P ≤ 0.0001, *** P ≤ 0.001, ** P ≤ 0.01, * P ≤ 0.05. b. Impact of silencing EGFR and downstream components of EGFR signalling pathway on the proliferation of Hs578T cells. Hs578T cells were transfected with siRNAs targeting EGFR, ERK2 and FRAP1 as well as positive (siKIF11) and negative controls (siGAPDH and siKinase Pool) as described and grown for 4 days. Proliferation was then assessed using sulphorhodamine B assay. Results were normalised to Kinase Pool using the % control method as described in materials and methods. (PDF 191 kb)