Skip to main content
. 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 3. Mutation of the palmitoylated cysteine 1025 of EGFR in combination with KrasG12V increases gefitinib sensitivity.

Figure 3

(A) NIH3T3 cells stably expressing inducible full length EGFRWT or EGFRC1025A or empty vector control (EV) with KrasWT (left) or KrasG12V (right). Immunoblotting with EGFR shows induced expression of EGFRWT and EGFRC1025A, and immunoblotting with HA shows expression of HA-tagged KrasG12V. (B) Induced expression of EGFRC1025A in NIH3T3 stably expressing KrasG12V increased gefitinib-induced cell death. 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. Cell viability was measured by Trypan Blue staining at 72 hours post-treatment (mean +/−StDev).