PAI-1过表达促进食管鳞癌细胞的侵袭和迁移

食管癌是常见的恶性肿瘤之一。由SERPINE1基因编码的纤溶酶原激活物抑制因子1(plasminogen activator inhibitor-1,PAI-1)已被报道在多种类型癌症患者的肿瘤组织中存在高表达并参与癌症进展。为探讨PAI-1蛋白在食管鳞癌中的作用及其分子机制,本研究首先利用Westernblot实验和酶联免疫吸附实验(enzyme linked immunosorbent assay, ELISA)检测各食管鳞癌细胞系中PAI-1的表达和分泌水平,结果显示,PAI-1高表达的食管鳞癌细胞系分泌至细胞外的PAI-1水平相对较高。进一步选取PAI-1表达及分泌水平均较高的KYSE150和KYSE450细胞系作为研究模型,通过si RNA(小干扰RNA)瞬时转染和Transwell实验证实敲降SERPINE1可显著抑制食管鳞癌KYSE150和KYSE450细胞的侵袭和迁移。同时,构建了慢病毒介导的SERPINE1稳定敲降细胞株KYSE150和KYSE450,将SERPINE1稳定敲降的细胞培养基中外源加入PAI-1蛋白进行Transwell回复实验,结果表明PAI-1过表达可增强食管鳞癌细胞的侵袭和迁移能力。体内实验结果显示,降低PAI-1表达可显著抑制食管鳞癌细胞的成瘤和肺转移能力。分子水平检测表明PAI-1过表达可激活AKT和ERK信号通路,免疫共沉淀(co-immunoprecipitation,Co-IP)实验结果进一步显示PAI-1可能与膜受体LRP1(LDLreceptor related protein1)存在相互作用。上述研究结果表明,PAI-1可能通过与LRP1相互作用进而促进食管鳞癌细胞的侵袭和迁移。

PAI-1 overexpression promotes invasion and migration of esophageal squamous carcinoma cells

Esophageal squamous cell carcinoma(ESCC) is one of the most common cancers worldwide. Plasminogen activator inhibitor-1(PAI-1), encoded by SERPINE1, is highly expressed in various types of tumor tissues, which contributes to cancer progression. The present study explored the role and underlying mechanisms of PAI-1 in ESCC. We found that the PAI-1 protein was extracellularly secreted more from ESCC cells with high PAI-1 expression using Western blotting and enzyme linked immunosorbent assay(ELISA). Knockdown of SERPINE1 expression significantly inhibited the invasion and migration of ESCC KYSE150 and KYSE450 cell lines, which could be restored when adding exogenous human recombinant PAI-1 into the culture medium of the cells stably expressing SERPINE1 sh RNA. In vivo experiments showed that SERPINE1 knockdown significantly inhibited xenograft growth and lung metastasis of ESCC cells. Molecular analysis demonstrated that PAI-1 activated AKT and ERK signaling pathways. Co-immunoprecipitation(Co-IP) assays identified that PAI-1 may interact with the membrane receptor LDL receptor related protein 1(LRP1). These results indicated that overexpression of PAI-1, through interacting with LRP1, might enhance invasion and migration of ESCC cells as well as promote ESCC progression.