Fu Y-N, Yeh C-L, Cheng H H-Y, Yang C-H, Tsai S-F, Huang S-F, Chen Y-R
Division of Molecular and Genomic Medicine, National Health Research Institutes, Zhunan, Taiwan, ROC.
Oncogene. 2008 Feb 7;27(7):957-65. doi: 10.1038/sj.onc.1210684. Epub 2007 Jul 23.
Mutations in epidermal growth factor receptor (EGFR) kinase domain associate with clinical responses to EGFR inhibitors and are frequently observed in non-small cell lung cancer (NSCLC) patients in East Asian populations. Clinically identified EGFR mutations cause constitutive receptor activation. The activating mechanisms were unclear but appeared to be different among EGFR mutants. We found that EGFR mutants had different sensitivity to an Src inhibitor PP2. S768I and L861Q mutants were less sensitive to Src suppression than others. Mutation at tyrosine 869 (845) residue, an Src phosphorylation site, decreased the phosphorylation levels of wild-type EGFR and other mutants, but not that of S768I and L861Q mutants, suggesting that S768I and L861Q mutants became Src independent for their activation and biological functions. In contrast, cells expressing EGFR-L858R or exon 19 deletion mutants were more sensitive to PP2 than cells expressing wild-type EGFR. Interestingly, EGFR with exon 19-deletion/T790M double mutations, which was resistant to gefitinib, remained sensitive to PP2. Taken together, our data indicate that Src inhibitors might be effective in treating NSCLC harboring specific types of EGFR mutations.
表皮生长因子受体(EGFR)激酶结构域的突变与EGFR抑制剂的临床反应相关,且在东亚人群的非小细胞肺癌(NSCLC)患者中经常观察到。临床鉴定的EGFR突变导致受体组成性激活。激活机制尚不清楚,但在EGFR突变体中似乎有所不同。我们发现EGFR突变体对Src抑制剂PP2具有不同的敏感性。S768I和L861Q突变体对Src抑制的敏感性低于其他突变体。Src磷酸化位点酪氨酸869(845)残基的突变降低了野生型EGFR和其他突变体的磷酸化水平,但不影响S768I和L861Q突变体的磷酸化水平,这表明S768I和L861Q突变体在激活和生物学功能上变得不依赖Src。相反,表达EGFR-L858R或外显子19缺失突变体的细胞比表达野生型EGFR的细胞对PP2更敏感。有趣的是,对吉非替尼耐药的外显子19缺失/T790M双突变的EGFR对PP2仍然敏感。综上所述,我们的数据表明Src抑制剂可能对治疗携带特定类型EGFR突变的NSCLC有效。