成纤维细胞生长因子受体1
血管生成
癌症研究
细胞生长
体内
A549电池
细胞凋亡
成纤维细胞生长因子
肺癌
体外
新生血管
肽
受体
成纤维细胞
化学
生物
医学
内科学
生物化学
生物技术
作者
Qiaoyan Tan,Zuqiang Wang,Quan Wang,Yuanqiang Wang,Zhifeng Huang,Nan Su,Min Jin,Liang Kuang,Huabing Qi,Zhenhong Ni,Can Li,Ying Zhu,Wanling Jiang,Hangang Chen,Chu‐Xia Deng,Xiaolan Du,Yangli Xie,Lin Chen
摘要
It has been reported that overactivation of fibroblast growth factor receptor 1 (FGFR1) is an important characteristic found in most non-small cell lung cancer (NSCLC) samples.Here, we identified a FGFR1 inhibitory peptide R1-P2 and investigated its effects on the lung cancer cells growth and angiogenesis in vitro and in vivo.Our results demonstrate that R1-P2 bound to human FGFR1 protein, and efficiently blocked the binding of FGF2 to FGFR1 in A549 and NCI-H460 cells.Moreover, this peptide significantly decreased the proliferation, migration and invasion, but promoted the apoptosis in both cell lines.In addition, R1-P2 treatment effectively inhibited the tumor growth and neovascularization in nude mice with xenografted A549 cells, and R1-P2 also significantly inhibited the FGF2-induced angiogenesis in tube formation experiment and CAM model.We further demonstrated that R1-P2 suppressed lung tumor growth through anti-angiogenic and anti-proliferative activity.Our data may provide a novle leading molecule with potential application in the treatment of FGFR1 activation related lung cancers.
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