Gene expression analysis of pancreatic cell lines reveals genes overexpressed in pancreatic cancer

被引:50
作者
Alldinger, I
Dittert, D
Peiper, M
Fusco, A
Chiappetta, G
Staub, E
Löhr, M
Jesnowski, R
Baretton, G
Ockert, D
Saeger, HD
Grützmann, R
Pilarsky, C
机构
[1] Univ Hosp Dresden, Dept Visceral Thorac & Vasc Surg, DE-01307 Dresden, Germany
[2] Univ Hosp Dresden, Dept Pathol, DE-01307 Dresden, Germany
[3] Univ Hosp, Dept Gen & Visceral Surg, Dusseldorf, Germany
[4] Univ Naples Federico II, Dipartimento Biol & Patol Cellulare & Mol, CNR, Ctr Endocrinol & Oncol Sperimentale, Naples, Italy
[5] Ist Tunori, Dept Expt Oncol, Naples, Italy
[6] Univ Hosp, Dept Med, Mannheim, Germany
[7] metaGen Pharmaceut, Berlin, Germany
关键词
pancreas; cancer; cell line; primary isolates; microarray; thymosin; immunohistochemistry;
D O I
10.1159/000086537
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Pancreatic cancer is one of the leading causes of cancer-related death. Using DNA gene expression analysis based on a custom made Affymetrix cancer array, we investigated the expression pattern of both primary and established pancreatic carcinoma cell lines. Methods: We analyzed the gene expression of 5 established pancreatic cancer cell lines (AsPC-1, BxPC-3, Capan-1, Capan-2 and HPAF II) and 5 primary isolates, 1 of them derived from benign pancreatic duct cells. Results: Out of 1,540 genes which were expressed in at least 3 experiments, we found 122 genes upregulated and 18 downregulated in tumor cell lines compared to benign cells with a fold change >3. Several of the upregulated genes (like Prefoldin 5, ADAM9 and E-cadherin) have been associated with pancreatic cancer before. The other differentially regulated genes, however, play a so far unknown role in the course of human pancreatic carcinoma. By means of immunohistochemistry we could show that thymosin beta-10 (TMSB10), upregulated in tumor cell lines, is expressed in human pancreatic carcinoma, but not in non-neoplastic pancreatic tissue, suggesting a role for TMSB10 in the carcinogenesis of pancreatic carcinoma. Conclusion: Using gene expression profiling of pancreatic cell lines we were able to identify genes differentially expressed in pancreatic adenocarcinoma, which might contribute to pancreatic cancer development. Copyright (C) 2005 S. Karger AG, Basel and IAP.
引用
收藏
页码:370 / 379
页数:10
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