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. Author manuscript; available in PMC: 2018 Nov 4.
Published in final edited form as: Biochem Biophys Res Commun. 2017 Sep 9;493(1):213–219. doi: 10.1016/j.bbrc.2017.09.044

Figure 1. Expression of palmitoylation defective EGFRC1025A mediates gefitinib-induced cytotoxicity.

Figure 1

(A) Gefitinib increases cytotoxicity in DHHC20 silenced Kras mutant cells MDA-MB-231. (B) MDA-MB-231 (KrasG13D) cells stably expressing inducible EGFRWT or EGFRC1025A or empty vector control (EV) were treated with doxocycline (1µg/ml) for 15 hours. Immunoblotting with anti-FLAG shows induced expression of FLAG tagged EGFRWT and EGFRC1025A. (C) Cells were treated with doxocycline (1µg/ml) every 24 hours for 72 hours and with DMSO or 5 µM gefitinib at 24 hours post-seeding. Expression of EGFRC1025A induced sensitivity to gefitinib. Cell viability was measured by Trypan Blue staining at 72 hours post-treatment (mean +/−StDev). (D) Induced expression of EGFRC1025A in MDA-MB-231 cells reduces cell growth.