Identification of Genomic Alterations Associated with the Aggressiveness of Pancreatic Cancer Using an Ultra-High-Resolution CGH Array

被引:7
|
作者
Legoffic, Aude [1 ]
Calvo, Ezequiel Luis [1 ,2 ]
Barthet, Marc [1 ]
Delpero, Jean-Robert [3 ]
Dagorn, Jean Charles [1 ]
Iovanna, Juan Lucio [1 ]
机构
[1] INSERM, U Stress Cellulaire 624, FR-13288 Marseille 9, France
[2] CHUL Res Ctr, Mol Endocrinol & Oncol Res Ctr, Quebec City, PQ, Canada
[3] Inst J Paoli I Calmettes, Dept Chirurg Oncol, F-13009 Marseille, France
关键词
Pancreatic adenocarcinoma; Genomic alterations; CGH array; Aggressiveness; Microarray; Affymetrix; CARCINOMA CELL-LINES; HOMOZYGOUS DELETIONS; GENETIC ALTERATIONS; COPY NUMBER; HYBRIDIZATION; ADENOCARCINOMA; EXPRESSION; AMPLIFICATIONS; ABERRATIONS; TARGET;
D O I
10.1159/000212092
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Genomic alterations present in pancreatic adenocarcinoma have been described only partially. In addition, the relations between these alterations and the aggressiveness of the phenotype remain unknown. Methods: Genomic DNA and total RNA from 5 pancreatic cell lines, of which 2 have an aggressive phenotype and are gemcitabine-resistant (Mia-Paca2 and Panc-1), and 3 less aggressive and gemcitabine-sensitive (Capan-1, Capan-2 and BxPC3), have been purified. DNA abnormalities have been analyzed using an ultra-high-resolution CGH array and mRNA expression was studied with an Affymetrix GeneChip expression array. Results: We identified 573 amplified and 30 deleted genes common to all 5 cell lines. Some of them have already been described, whereas other genes, implicated in signal transduction, apoptosis, cell cycle or cell migration, are described for the first time as being related to this cancer. Comparison of genomic abnormalities between the 2 most aggressive and the 3 less aggressive cell lines led to the identification of 368 genes specifically amplified in the aggressive cell lines. However, no specific gene deletion seems to be associated with the aggressive phenotype. Conclusion: Using a high-resolution approach, we could precisely describe the genomic alterations associated with pancreatic adenocarcinoma and determine those associated with an aggressive phenotype. Copyright (C) 2009 S. Karger AG, Basel and IAP
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页码:267 / 272
页数:6
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