Grützmann Robert, Foerder Melanie, Alldinger Ingo, Staub Eike, Brümmendorf Thomas, Röpcke Stefan, Li Xinzhong, Kristiansen Glen, Jesenofsky Ralf, Sipos Bence, Löhr Matthias, Lüttges Jutta, Ockert Detlef, Klöppel Günter, Saeger Hans Detlev, Pilarsky Christian
Department of Visceral, Thoracic and Vascular Surgery, University Hospital Carl Gustav Carus, Technical University of Dresden, Germany.
Virchows Arch. 2003 Oct;443(4):508-17. doi: 10.1007/s00428-003-0884-1. Epub 2003 Aug 27.
In a search for new molecular markers of pancreatic ductal adenocarcinoma (PDAC), we compared the gene expression profiles of seven pancreatic carcinomas and one carcinoma of the papilla Vateri with those of duct cells from three non-neoplastic pancreatic tissues. In addition, the human pancreatic duct cell line and five PDAC cell lines (AsPC-1, BxPC-3, Capan-1, Capan-2, HPAF) were examined. RNA was extracted from microdissected tissue or cultured cell lines and analysed using a custom-made Affymetrix Chip containing 3023 genes, of which 1000 were known to be tumour associated. Hierarchical clustering revealed 81 differentially expressed genes. Of all the genes, 26 were downregulated in PDAC and 14 were upregulated in PDAC. In PDAC cell lines versus normal pancreatic duct cells, 21 genes were downregulated and 20 were upregulated. Of these 81 differentially expressed genes, 15 represented human genes previously implicated in the tumourigenesis of PDAC. From the genes that were so far not known to be associated with PDAC tumorigenesis, we selected ADAM9 for further validation because of its distinct overexpression in tumour tissue. Using immunohistochemistry, the over-expressed gene, ADAM9, was present in 70% of the PDACs analysed. In conclusion, using microarray technology we were able to identify a set of genes whose aberrant expression was associated with PDAC and may be used to target the disease.
为寻找胰腺导管腺癌(PDAC)新的分子标志物,我们比较了7例胰腺癌和1例 Vateri 乳头癌与3个非肿瘤性胰腺组织导管细胞的基因表达谱。此外,还检测了人胰腺导管细胞系和5种PDAC细胞系(AsPC-1、BxPC-3、Capan-1、Capan-2、HPAF)。从显微切割的组织或培养的细胞系中提取RNA,并使用定制的包含3023个基因的Affymetrix芯片进行分析,其中1000个基因已知与肿瘤相关。层次聚类显示81个差异表达基因。在所有基因中,26个在PDAC中下调,14个在PDAC中上调。在PDAC细胞系与正常胰腺导管细胞相比中,21个基因下调,20个基因上调。在这81个差异表达基因中,15个代表先前与PDAC肿瘤发生相关的人类基因。从目前尚不知与PDAC肿瘤发生相关的基因中,我们选择ADAM9进行进一步验证,因为它在肿瘤组织中明显过表达。使用免疫组织化学方法,分析的PDAC中有70%存在过表达基因ADAM9。总之,利用微阵列技术我们能够鉴定出一组基因,其异常表达与PDAC相关,可能用于靶向治疗该疾病。