Primary antibodies against ErbB2 (C-18; sc-284), phospho-ErbB2 (Tyr1248; sc-12352-R), ErbB1 (1005; sc-03), and phospho-ErbB1 (Tyr1173; sc-12351)

were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA). Primary antibodies against phospho-Akt (Ser 473; #9271), Akt (#9272), phospho-p42/44 mitogen-activated protein kinase (MAPK) (Thr202/Thr204; #4377), p42/44 MAPK (#9102), caspase-3 (#9662), and cyclin D1 (#2926) were purchased from Cell Signaling Technology (Beverly, MA). Anti-actin (A 2066) was obtained from Sigma Aldrich Co. http://www.selleckchem.com/products/FK-506-(Tacrolimus).html (St. Louis, MO). Tryphostin AG879 and tryphostin AG1517 were purchased from Calbiochem-Novabiochem Corp. (San Diego, CA). Lapatinib was kindly provided by GlaxoSmithKline, Inc. (Research Triangle Park, NC). The rat cholangiocarcinoma cell lines C611B and BDEneu were each generated in our laboratory and have been previously described.3-5 The human cholangiocarcinoma cell line, HuCCT1, was purchased from Acalabrutinib in vitro the Japan Health Science Foundation (Osaka, Japan). TFK1, the other human cholangiocarcinoma cell line used in this study, was purchased from the German Collection of Microorganisms and

Cell Cultures (Braunschweig, Germany). All of the cholangiocarcinoma cell lines used in this study, with the exception of the HuCCT1 cell line, were cultured in Dulbecco’s modified Eagle medium (DMEM) supplemented according to our standard culture conditions.3 HuCCT1 cells were cultured under comparable conditions in Roswell Park Memorial Institute 1640 (RPMI-1640) medium. In vitro drug treatments with tryphostins AG879 and AG1517, alone and in combination, as well as with lapatinib,

were carried out against the various rat and human cholangiocarcinoma cell lines maintained in culture in either DMEM or RPMI-1640 medium in the presence of 2.5% fetal bovine serum. A range of concentrations of each TK GABA Receptor dissolved in dimethyl sulfoxide (DMSO; final DMSO concentration per culture = 0.1%) were added to the culture medium of the drug-treated cultures, beginning at 16-24 hours after initial cell plating and then continuing daily for up to an additional 72 hours, depending on the experimental design. Vehicle control cultures were exposed to 0.1% DMSO only. In vitro cell growth was assessed using the CellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay Kit from Promega Corp. (Madison, WI), as described.4, 6 Western blot analysis of total protein in cell lysates prepared from vehicle control and ErbB TK inhibitor–treated cholangiocarcinoma cell lines was also performed as described,4, 7 using commercially available antibodies that had been validated by us for reactivity and specificity.