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2 protocols using masatinib

1

Multidrug-resistant Oral Cancer Cell Lines

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Rhodamine123 (Rhodamine) and verapamil were purchased from Sigma-Aldrich (St. Louis, MO, USA). VIC was purchased from Enzo Life Sciences (Farmingdale, NY, USA). Gefitinib, imatinib, erlotinib, nilotinib, pazopanib, masatinib, sunitinib, sorafenib, regorafenib, lapatinib, vandetanib, cediranib, and crizotinib were purchased from Selleckchem (Houston, TX, USA). For in vivo xenograft experiments, VIC was purchased from APExBIO technology (TX, USA) and crizotinib was purchased from MedChemExpress (NJ, USA). Aqueous solutions of eribulin (Eisai Korea, Seoul, South Korea) were obtained from the National Cancer Center in South Korea.
Human oral squamous carcinoma cell line, parent sensitive KB, and its multidrug-resistant subline, KBV20C, were obtained from Dr. Yong Kee Kim (College of Pharmacy, Sookmyung Women's University, Seoul, South Korea) and have been previously described (12 (link), 29 (link)–31 (link)). All cell lines were cultured in RPMI 1640 containing 10% fetal bovine serum, 100 U/ml penicillin, and 100 μg/ml streptomycin (WelGENE, Daegu, South Korea).
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2

Fibrocyte Characterization and Migration

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We used immunofluorescence or flow cytometry to examine the protein expression of c-Abl, PDGFR-α, PDGFR-β, and c-Kit by murine or human fibrocytes. Migration of fibrocytes was assessed by using Boyden chambers coated with collagen I, as previously described. 26, 27 Recombinant human PDGF-AA, PDGF-BB, and stem cell factor were used as the chemoattractants. Differentiation of fibrocytes was assessed as previously described. 28 Imatinib or other inhibitors, such as nilotinib (c-Abl inhibitor), crenolanib (PDGFR inhibitor), or masatinib (c-Kit inhibitor; Selleck Chemicals) were used at the appropriate concentrations. Additional details are provided in the Supplementary material (available online at www.jhltonline.org.).
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