Luo Caifeng, Sun Fengying, Zhu Hong, Ni Ying, Fang Jian, Liu Yun, Shao Shihe, Shen Hongxing, Hu Jianpeng
School of Medicine, Jiangsu University, 301 Xuefu Road, Zhenjiang, Jiangsu 212013, PR China.
Department of Clinical Laboratory, The Second People's Hospital of Wuhu, 259 Jiuhuashan Road, Wuhu, Anhui 241000, PR China.
Pathol Res Pract. 2017 Sep;213(9):1029-1036. doi: 10.1016/j.prp.2017.08.009. Epub 2017 Aug 25.
Insulin-like growth factor binding protein-1 (IGFBP-1), a secreted protein, implicated of various cells in mediating the proliferation, migration, invasion, adhesion, survival and so on. In this study, we assessed the expression and release of IGFBP-1 from gastric cancer cells with H. pylori 26695 infection and the biological functions of IGFBP-1 in gastric cancer cells. The results showed that the expression and release of IGFBP-1 were increased in gastric cancer cells (MGC-803, BGC-823, SGC-7901) infected with H. pylori 26695. In addition, the upregulation of IGFBP-1 was dose-dependent in BGC-823 cells infected with H. pylori 26695 but not time-dependent. The upregulation of IGFBP-1 got to peak at 12h after H. pylori 26695 infection and then decreased over time. Subsequently, we measured its functions by silencing and overexpressing IGFBP1 which suggested that overexpression of IGFBP-1 could inhibit the migration of BGC-823 and SGC-7901 cells. However, knocking down the IGFBP-1 could increase the migration of BGC-823 and SGC-7901 cells. Functional findings illustrated that IGFBP-1 was implicated in H. pylori 26695-induced MMP-9 expression in BGC-823 cells. In addition, overexpressing IGFBP1 reduce the promoting effect of MMP-9 on the BGC-823 cells migration. In summary, we demonstrated that IGFBP-1 suppress the migration of BGC-823 cells and play a protective role in the process of H. pylori-induced gastric cancer.
胰岛素样生长因子结合蛋白-1(IGFBP-1)是一种分泌蛋白,参与多种细胞的增殖、迁移、侵袭、黏附、存活等过程。在本研究中,我们评估了幽门螺杆菌26695感染的胃癌细胞中IGFBP-1的表达和释放情况,以及IGFBP-1在胃癌细胞中的生物学功能。结果显示,幽门螺杆菌26695感染的胃癌细胞(MGC-803、BGC-823、SGC-7901)中IGFBP-1的表达和释放增加。此外,幽门螺杆菌26695感染的BGC-823细胞中IGFBP-1的上调呈剂量依赖性,而非时间依赖性。幽门螺杆菌26695感染后12小时IGFBP-1上调达到峰值,随后随时间下降。随后,我们通过沉默和过表达IGFBP1来检测其功能,结果表明IGFBP-1过表达可抑制BGC-823和SGC-7901细胞的迁移。然而,敲低IGFBP-1可增加BGC-823和SGC-7901细胞的迁移。功能研究结果表明,IGFBP-1参与了幽门螺杆菌26695诱导的BGC-823细胞中MMP-9的表达。此外,过表达IGFBP1可降低MMP-9对BGC-823细胞迁移的促进作用。总之,我们证明了IGFBP-1抑制BGC-823细胞的迁移,并在幽门螺杆菌诱导的胃癌过程中发挥保护作用。