作者: Barbara Fischer , Marin Marinov , Alexandre Arcaro
DOI: 10.1016/J.CTRV.2007.01.006
关键词: Epidermal growth factor receptor 、 Medicine 、 Metastasis 、 Protein kinase B 、 Receptor tyrosine kinase 、 Lung cancer 、 Cancer research 、 PI3K/AKT/mTOR pathway 、 Phosphoinositide 3-kinase 、 Pharmacology 、 Gefitinib
摘要: Small cell lung cancer (SCLC) is an aggressive form of cancer, which represents 13% all cases and strongly associated with cigarette smoking. The survival SCLC patients dismal has not greatly improved in the last 20 years, despite advances chemotherapy regimens a better understanding biology. development resistance to metastasis are commonly recognized as important causes poor clinical outcome SCLC. Targeting receptor tyrosine kinase (RTK) signalling attractive approach develop new drugs for SCLC, view accumulating data demonstrating that polypeptide growth factors play key role driving proliferation, chemoresistance metastasis. insulin-like factor-I (IGF-IR), c-Kit, vascular endothelial factor (VEGFR) epidermal (EGFR) have been identified potential drug targets Moreover, downstream mediators RTKs, such phosphoinositide 3-kinase (PI3K)/Akt mammalian target rapamycin (mTOR) may also represent candidate molecules anti-cancer therapies Here we will review available concerning results RTK inhibitors trials undertaken investigate these compounds anti-tumour agents