Microarray analysis of differentially expressed genes of primary tumors in the canine central nervous system

被引:34
|
作者
Thomson, SAM
Kennerly, E
Olby, N
Mickelson, JR
Hoffmann, DE
Dickinson, PJ
Gibson, G
Breen, M
机构
[1] N Carolina State Univ, Coll Vet Med, Dept Mol Biomed Sci, Raleigh, NC 27606 USA
[2] N Carolina State Univ, Coll Agr & Life Sci, Dept Genet, Raleigh, NC 27606 USA
[3] N Carolina State Univ, Coll Vet Med, Dept Clin Sci, Raleigh, NC 27606 USA
[4] Univ Minnesota, Coll Vet Med, Dept Vet Pathobiol, St Paul, MN 55108 USA
[5] Univ Calif Davis, Sch Vet Med, Dept Surg & Radiol Sci, Davis, CA USA
关键词
cDNA microarray; canine choroid plexus tumor; ependymoma; glial tumor; meningioma;
D O I
10.1354/vp.42-5-550
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The pathophysiologic similarities of many human and canine cancers support the role of the domestic dog as a model for brain tumor research. Here we report the construction of a custom canine brain-specific cDNA microarray and the analysis of gene expression patterns of several different types of canine brain tumor. The microarray contained 4000 clones from a canine brain specific cDNA library including 2161 clones that matched known genes or expressed sequence tags (ESTs) and 25 cancer-related genes. Our study included 16 brain tumors (seven meningiomas, five glial tumors, two ependymomas, and two choroid plexus papillomas) from a variety of different dog breeds. We identified several genes previously found to be differentially expressed in human brain tumors. This suggests that human and canine brain tumors share a common pathogenesis. In addition, we also found differentially expressed genes unique to either meningiomas or the glial tumors. This report represents the first global gene expression analysis of different types of canine brain tumors by cDNA microarrays and might aid in the identification of potential candidate genes involved in tumor formation and progression.
引用
收藏
页码:550 / 558
页数:9
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