Klein Shoshana, Levitzki Alexander
Unit of Cellular Signaling, Department of Biological Chemistry, The Hebrew University of Jerusalem, Givat Ram, Jerusalem, Israel.
Curr Opin Cell Biol. 2009 Apr;21(2):185-93. doi: 10.1016/j.ceb.2008.12.006. Epub 2009 Feb 11.
The EGFR and PKB pathways are frequently activated in cancer, so are prime targets for cancer therapy. To this end, new inhibitors are being tested. EGFR inhibitors as single therapy have little benefit, although therapies that evoke an antitumor immune response are more effective. Resistance mutations within the EGFR are common, as is activation of the antiapoptotic PKB pathway via alternative tyrosine kinase receptors, especially other EGFR family members or IGF1R. To combat resistance, multitargeted EGFR inhibitors and combined inhibition of the EGFR and PKB are being investigated. Inhibition of the EGFR and PKB pathways also sensitizes cancer cells to chemotherapy. Thus, EGFR and PI3K/PKB inhibitors will be most effective when used in rational combinations of targeted inhibitors and traditional chemotherapy.
表皮生长因子受体(EGFR)和蛋白激酶B(PKB)通路在癌症中经常被激活,因此是癌症治疗的主要靶点。为此,新的抑制剂正在进行测试。尽管能引发抗肿瘤免疫反应的疗法更有效,但EGFR抑制剂作为单一疗法益处不大。EGFR内的耐药性突变很常见,通过替代酪氨酸激酶受体激活抗凋亡PKB通路的情况也很常见,尤其是其他EGFR家族成员或胰岛素样生长因子1受体(IGF1R)。为了对抗耐药性,正在研究多靶点EGFR抑制剂以及EGFR和PKB的联合抑制。抑制EGFR和PKB通路也会使癌细胞对化疗敏感。因此,当EGFR和PI3K/PKB抑制剂与靶向抑制剂和传统化疗合理联合使用时,将最有效。