Expression of the thrombin receptor PAR-1 correlates with tumour cell differentiation of pancreatic adenocarcinoma in vitro

被引:50
|
作者
Rudroff, C
Seibold, S
Kaufmann, R
Cu Zetina, C
Reise, K
Schäfer, U
Schneider, A
Brockmann, M
Scheele, J
Neugebauer, EAM
机构
[1] Univ Cologne, Dept Surg 2, Biochem & Expt Div, D-51109 Cologne, Germany
[2] Hosp Cologne Merheim, Dept Med, Cologne, Germany
[3] Univ Jena, Dept Surg, D-6900 Jena, Germany
[4] Hosp Cologne Merheim, Dept Pathol, Cologne, Germany
关键词
cancer cell differentiation; gene expres- sion; pancreatic cancer; PAR-1; protein expression; thrombin receptor;
D O I
10.1023/A:1014598904644
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with pancreatic cancer frequently suffer from thrombosis due to excess thrombin generation. Yet, the effects of thrombin on pancreatic cancer are still poorly understood. The thrombin receptor PAR-1 is responsible for cellular effects of thrombin. PAR-1 plays an important role in the progression of different solid tumours in vitro. In breast cancer the level of PAR-1 expression correlates with invasiveness. Our aim was to correlate PAR-1 mRNA and protein expression level with the grade of differentiation of pancreatic tissue and cancer cell lines. PAR-1 protein was not detectable in the epithelium of healthy pancreas. Analysis of PAR-1 protein expression by immunofluorescence staining of pancreatic cancer cell lines revealed a correlation to the grade of differentiation. Quantitative analysis of PAR-1 protein expression by Western Blot analysis confirmed these observations. Analysis of PAR-1 mRNA expression showed low levels in healthy pancreas compared to pancreatic cancer tissue and the pancreatic cancer cell line MIA PaCa-2. The level of PAR-1 mRNA differed up to 25 fold between the respective pancreatic cancer cell lines. The eminent differences in PAR-1 expression, both protein and mRNA, between healthy pancreatic tissue and pancreatic cancer in vivo and in vitro emphasise the putative role of PAR-1 in pancreatic cancer progression.
引用
收藏
页码:181 / 189
页数:9
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