Pilarsky Christian, Ammerpohl Ole, Sipos Bence, Dahl Edgar, Hartmann Arndt, Wellmann Axel, Braunschweig Till, Löhr Matthias, Jesenofsky Ralf, Friess Helmut, Wente Moritz Nicolas, Kristiansen Glen, Jahnke Beatrix, Denz Axel, Rückert Felix, Schackert Hans K, Klöppel Günter, Kalthoff Holger, Saeger Hans Detlev, Grützmann Robert
Department of Visceral-, Thoracic- and Vascular Surgery, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
J Cell Mol Med. 2008 Dec;12(6B):2823-35. doi: 10.1111/j.1582-4934.2008.00289.x. Epub 2008 Feb 24.
Pancreatic ductal adenocarcinoma (PDAC) is characterized by an abundant desmoplastic stroma. Interactions between cancer and stromal cells play a critical role in tumour invasion, metastasis and chemoresistance. Therefore, we hypothesized that gene expression profile of the stromal components of pancreatic carcinoma is different from chronic pancreatitis and reflects the interaction with the tumour. We investigated the gene expression of eleven stromal tissues from PDAC, nine from chronic pancreatitis and cell lines of stromal origin using the Affymetrix U133 GeneChip set. The tissue samples were microdissected, the RNA was extracted, amplified and labelled using a repetitive in vitro transcription protocol. Differentially expressed genes were identified and validated using quantitative RT-PCR and immuno-histochemistry. We found 255 genes to be overexpressed and 61 genes to be underexpressed within the stroma of pancreatic carcinoma compared to the stroma of chronic pancreatitis. Analysis of the involved signal transduction pathways revealed a number of genes associated with the Wnt pathway of which the differential expression of SFRP1 and WNT5a was confirmed using immunohistochemistry. Moreover, we could demonstrate that WNT5a expression was induced in fibroblasts during cocultivation with a pancreatic carcinoma cell line. The identified differences in the expression profile of stroma cells derived from tumour compared to cells of inflammatory origin suggest a specific response of the tissue surrounding malignant cells. The overexpression of WNT5a, a gene involved in the non canonical Wnt signalling and chondrocyte development might contribute to the strong desmoplastic reaction seen in pancreatic cancer.
胰腺导管腺癌(PDAC)的特征是有丰富的促结缔组织增生性基质。癌细胞与基质细胞之间的相互作用在肿瘤侵袭、转移和化疗耐药中起关键作用。因此,我们推测胰腺癌基质成分的基因表达谱与慢性胰腺炎不同,并反映了与肿瘤的相互作用。我们使用Affymetrix U133基因芯片组研究了来自PDAC的11个基质组织、来自慢性胰腺炎的9个基质组织以及基质来源的细胞系的基因表达。对组织样本进行显微切割,提取RNA,使用重复体外转录方案进行扩增和标记。使用定量RT-PCR和免疫组织化学鉴定并验证差异表达基因。我们发现与慢性胰腺炎的基质相比,胰腺癌基质中有255个基因过表达,61个基因低表达。对所涉及的信号转导途径的分析揭示了许多与Wnt途径相关的基因,其中SFRP1和WNT5a的差异表达通过免疫组织化学得到证实。此外,我们可以证明在与胰腺癌细胞系共培养期间,成纤维细胞中WNT5a表达被诱导。与炎症来源的细胞相比,肿瘤来源的基质细胞表达谱的差异表明恶性细胞周围组织有特异性反应。WNT5a是一种参与非经典Wnt信号传导和软骨细胞发育的基因,其过表达可能导致胰腺癌中强烈的促结缔组织增生反应。