Skip to main content
. 2011 Oct 4;105(10):1542–1553. doi: 10.1038/bjc.2011.400

Table 2. Drugs used and their IC50 values (μM) in MPM cells.

Drugs Drug targets H2052 H2452 H28 MSTO-211H
Carboplatin DNA 5.30±1.02 2.69±0.71 10.50±2.59 0.51±0.12
Pemetrexed TS, DHFR, GARFT 0.07±0.01 2.82±0.17 10.96±2.46 0.02±0.01
Vandetanib EGFR, VEGFR-2/3, RET 1.07±0.04 3.52±1.13 0.32±0.07 1.42±0.03
Sorafenib Raf, PDGF, VEGFR-2/3 6.09±1.78 14.59±4.58 10.22±1.93 3.18±0.27
Gefitinib EGFR 5.22±1.53 4.83±1.24 3.99±1.28 4.91±1.04
Erlotinib EGFR 5.55±1.28 5.26±1.29 3.92±1.06 5.48±1.93
Enzastaurin PKCβ, VEGF 11.56±3.82 10.07±2.96 8.11±2.19 10.92±2.59
ZM447439 Aurora kinase B 12.73±3.49 10.40±3.27 11.12±4.02 9.65±3.06

Abbreviations: DHFR=dihydrofolate reductase; DMSO=dimethyl sulfoxide; EGFR=epidermal growth factor receptor; GARFT=glycinamide ribonucleotide formyltransferase; MTT=3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; PDGF=platelet-derived growth factor; PKCβ=protein kinase Cβ; RET=rearranged during transfection; SRB=sulforhodamine B; TS=thymidylate synthase; VEGFR=vascular endothelial growth factor receptor; MPM=malignant pleural mesothelioma.

Notes: The drugs were dissolved in DMSO or sterile water and diluted in culture medium before use. IC50 concentrations were calculated as mean values±s.e.m. of at least three independent MTT or SRB experiments.