Department of Developmental Biology, Key Laboratory of Cell Biology, Ministry of Public Health and Key Laboratory of Medical Cell Biology, Ministry of Education, China Medical University, Shenyang, China.
Oncogene. 2013 Jun 13;32(24):2952-62. doi: 10.1038/onc.2012.313. Epub 2012 Jul 16.
Brain metastasis (BM) is a major cause of mortality in small-cell lung cancer (SCLC) patients; however, the molecular pathway of SCLC BM remains largely unknown because of a lack of investigation. Here we screen the levels of some candidate-soluble factors in the serum of SCLC patients and find that SCLC patients with high levels of placental growth factor (PLGF) are prone to BM. Using in vitro blood-brain barrier model, we show that PLGF derived from SCLC cells triggers vascular endothelial growth factor receptor-1-Rho-extracellular regulated protein kinase 1/2 signaling axis activation, results in disassembly of tight junction in brain endothelial cells and promotes SCLC cell transendothelial migration. Furthermore, the downregulation of PLGF suppresses SCLC cell metastasis to the brain in an experimental BM model. These data suggest that PLGF is a potential signature of SCLC BM and a prospective therapeutic target for SCLC BM.
脑转移(BM)是小细胞肺癌(SCLC)患者死亡的主要原因;然而,由于缺乏研究,SCLC BM 的分子途径在很大程度上仍不清楚。在这里,我们筛选了 SCLC 患者血清中的一些候选可溶性因子的水平,发现 PLGF 水平较高的 SCLC 患者易发生 BM。通过体外血脑屏障模型,我们表明 SCLC 细胞衍生的 PLGF 触发血管内皮生长因子受体-1-Rho-细胞外调节蛋白激酶 1/2 信号轴的激活,导致脑内皮细胞紧密连接解体,并促进 SCLC 细胞穿越内皮迁移。此外,PLGF 的下调抑制了实验性 BM 模型中 SCLC 细胞向脑的转移。这些数据表明 PLGF 是 SCLC BM 的一个潜在标志物,也是 SCLC BM 的一个有前途的治疗靶点。