瞄准:探索肌动朊捆绑蛋白质的角色, fascin 在胰腺的癌症的前进期间。方法:表示人的 fascin-1 的 plasmid 是稳定地 transfected 进胰腺的癌症房间线 MIA PaCa-2。增长,房间周期,活动性,散布,在 fascin-transfected MIA PaCa-2 房间和控制 non-transfected 房间的肌动朊细丝系统的侵略和组织被决定。结果:fascin 的异构的 overexpression 显著地提高了活动性,散布,并且 MIA PaCa-2 房间的侵略。然而, fascin 的 overexpression 在 MIA PaCa-2 房间增长和房间周期上有最小的效果。另外,肌动朊细丝系统的房间形态学和组织清楚地在 fascin overexpressed 房间被改变。当移植了进 BALB/c-nu 老鼠时,胰腺的癌症房间开发了的 fascin-transfected 以稍微更慢的率的稳固的肿瘤,而是这些肿瘤与控制肿瘤比较显示了更多的好攻击的行为。结论:Fascin 支持胰腺的癌症房间移植,侵略并且散布,因此贡献胰腺的癌症房间的好攻击的行为。
AIM: To explore the role of actin-bundling protein, fascin during the progression of pancreatic cancer,METHODS: The plasmid expressing human fascin-1 was stably transfected into the pancreatic cancer cell line MIA PaCa-2. The proliferation, cell cycle, motility, scattering, invasiveness and organization of the actin filament system in fascin-transfected MIA PaCa-2 cells and control non-transfected cells were determined.RESULTS: Heterogeneous overexpression of fascin markedly enhanced the motility, scattering, and inva-siveness of MIA PaCa-2 cells. However, overexpression of fascin had minimal effect on MIA PaCa-2 cell pro- liferation and cell cycle. In addition, cell morphology and organization of the actin filament system were distinctly altered in fascin overexpressed cells. When transplanted into BALB/c-nu mice, fascin-transfected pancreatic cancer cells developed solid tumors at a slightly slower rate, but these tumors displayed more aggressive behavior in comparison with control tumors.CONCLUSION: Fascin promotes pancreatic cancer cell migration, invasion and scattering, thus contributes to the aggressive behavior of pancreatic cancer cells.