Neural invasion in pancreatic cancer:: A mutual tropism between neurons and cancer cells

被引:110
作者
Ceyhan, Gueralp O. [1 ]
Demir, Ihsan Ekin [1 ]
Altintas, Burak [2 ]
Rauch, Ulrich [3 ]
Thiel, Gerald [4 ]
Mueller, Michael W. [1 ]
Giese, Nathalia A. [2 ]
Friess, Helmut [1 ]
Schaefer, Karl-Herbert [3 ]
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Surg, D-81675 Munich, Germany
[2] Heidelberg Univ, Dept Gen Surg, D-6900 Heidelberg, Germany
[3] Univ Appl Sci, Dept Biotechnol, Kaiserslautern, Germany
[4] Univ Saarland, Med Ctr, Dept Med Biochem & Mol Biol, D-6650 Homburg, Germany
关键词
neural invasion; pancreatic cancer; in-vitro migration; myenteric plexus; dorsal root ganglia; NGF; GDNF; artemin; persephin; neurturin;
D O I
10.1016/j.bbrc.2008.07.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neural invasion by pancreatic cancer cells (PCC) worsens the prognosis and frequently limits curative resection. We established a novel in-vitro model in which T3M4-PCCs were co-cultured with either isolated myenteric plexus cells (MP) or dorsal root ganglia (DRG) of newborn rats within a three-dimensional extracellular matrix gel. The close vicinity of MP or DRG to T3M4-PCCs induced early morphologic changes on T3M4-PCCs at the migration front prior to the migration process with elongated and neurite-targeting PCCs, compared to round and non-grouping at the non-migrating front. T3M4-PCCs built cancer-cell clusters around the DRG or MP, a process which was accelerated by increasing number of T3M4-PCCs or neurons. These findings indicate that neuro-cancer interactions start prior to PCC migration and induce evident changes in cancer and nerve biology. These findings can be reproduced within the introduced 3D in-vitro migration assay which allows investigation in the early pathogenesis of neural PCC invasion. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:442 / 447
页数:6
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