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


Ceyhan G., Demir I. E., Altintas B., Rauch U., Thiel G., Mueller M. W., ...More

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, vol.374, no.3, pp.442-447, 2008 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 374 Issue: 3
  • Publication Date: 2008
  • Doi Number: 10.1016/j.bbrc.2008.07.035
  • Journal Name: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED)
  • Page Numbers: pp.442-447
  • Keywords: neural invasion, pancreatic cancer, in-vitro migration, myenteric plexus, dorsal root ganglia, NGF, GDNF, artemin, persephin, neurturin, PERINEURAL INVASION, MYENTERIC PLEXUS, EXPRESSION, GROWTH
  • Acibadem Mehmet Ali Aydinlar University Affiliated: No

Abstract

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.