%0 Journal Article
%T Gefitinib (IRESSA) sensitive lung cancer cell lines show phosphorylation of Akt without ligand stimulation
%A Rintaro Noro
%A Akihiko Gemma
%A Seiji Kosaihira
%A Yutaka Kokubo
%A Mingwei Chen
%A Masahiro Seike
%A Kiyoko Kataoka
%A Kuniko Matsuda
%A Tetsuya Okano
%A Yuji Minegishi
%A Akinobu Yoshimura
%A Shoji Kudoh
%J BMC Cancer
%D 2006
%I BioMed Central
%R 10.1186/1471-2407-6-277
%X To identify other key factors involved in gefitinib sensitivity, we analyzed the protein expression of molecules within the EGFR family, PI3K-Akt and Ras/MEK/Erk pathways and examined the sensitivity to gefitinib using the MTT cell proliferation assay in 23 lung cancer cell lines.We identified one highly sensitive cell line (PC9), eight cell lines displaying intermediate-sensitivity, and 14 resistant cell lines. Only PC9 and PC14 (intermediate-sensitivity) displayed an EGFR gene mutation including amplification. Eight out of the nine cell lines showing sensitivity had Akt phosphorylation without ligand stimulation, while only three out of the 14 resistant lines displayed this characteristic (P = 0.0059). Furthermore, the ratio of phosphor-Akt/total Akt in sensitive cells was higher than that observed in resistant cells (P = 0.0016). Akt phosphorylation was partially inhibited by gefitinib in all sensitive cell lines.These results suggest that Akt phosphorylation without ligand stimulation may play a key signaling role in gefitinib sensitivity, especially intermediate-sensitivity. In addition, expression analyses of the EGFR family, EGFR gene mutation, and FISH (fluorescence in situ hybridization) analyses showed that the phosphorylated state of EGFR and Akt might be a useful clinical marker of Akt activation without ligand stimulation, in addition to EGFR gene mutation and amplification, particularly in adenocarcinomas.Gefitinib(IRESSA) [4-(3-chloro-4-fluoroanilino)-7-methoxy-6-(3-morpholinopropoxy)-quinazoline] is an orally active, epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor that inhibits EGFR signaling [1,2]. IDEAL (IRESSA Dose Evaluation in Advanced Lung cancer) 1 and 2 were randomized Phase II trials in patients with non-small cell lung cancer (NSCLC) refractory to platinum-based chemotherapy. These trials demonstrated that gefitinib was active and generally well tolerated [3,4]. However, ISEL (IRESSA Survival Evaluation in Lung cancer), a
%U http://www.biomedcentral.com/1471-2407/6/277