Gene expression patterns and gene copy number changes in dermatofibrosarcoma protuberans

被引:108
作者
Linn, SC
West, RB
Pollack, JR
Zhu, S
Hernandez-Boussard, T
Nielsen, TO
Rubin, BP
Patel, R
Goldblum, JR
Siegmund, D
Botstein, D
Brown, PO
Gilks, CB
van de Rijn, M
机构
[1] Stanford Univ, Med Ctr, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Med Ctr, Dept Genet, Stanford, CA 94305 USA
[3] Stanford Univ, Med Ctr, Dept Biochem, Stanford, CA 94305 USA
[4] Stanford Univ, Med Ctr, Howard Hughes Med Inst, Stanford, CA 94305 USA
[5] Cleveland Clin Fdn, Dept Anat Pathol, Cleveland, OH 44195 USA
[6] Univ Washington, Med Ctr, Dept Anat Pathol, Seattle, WA 98195 USA
[7] Vancouver Gen Hosp, Genet Pathol Evaluat Ctr, Vancouver, BC, Canada
[8] Vancouver Gen Hosp, Dept Pathol, Vancouver, BC, Canada
[9] Stanford Univ, Dept Stat, Stanford, CA 94305 USA
关键词
D O I
10.1016/S0002-9440(10)63593-6
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Dermatofibrosarcoma protuberans (DFSP) is an aggressive spindle cell neoplasm. it is associated with the chromosomal translocation, t(17:22), which fuses the COL1A1 and PDGFbeta genes. We determined the characteristic gene expression profile of DFSP and characterized DNA copy number changes in DFSP by array-based comparative genomic hybridization (array CGH). Fresh frozen and formalin-fixed, paraffin-embedded samples of DFSP were analyzed by array CGH (four cases) and DNA microarray analysis of global gene expression (nine cases). The nine DFSPs were readily distinguished from 27 other diverse soft tissue tumors based on their gene expression patterns. Genes characteristically expressed in the DFSPs included PDGFbeta and its receptor, PDGFRB, APOD, MEOX1, PLA2R, and PRKCA. Array CGH of DNA extracted either from frozen tumor samples or from paraffin blocks yielded equivalent results. Large areas of chromosomes 17q and 22q, bounded by COL1A1 and PDGFbeta, respectively, were amplified in DFSP. Expression of genes in the amplified regions was significantly elevated. Our data shows that: 1) DFSP has a distinctive gene expression profile; 2) array CGH can be applied successfully to frozen or formalin-fixed, paraffin-embedded tumor samples; 3) a characteristic amplification of sequences from chromosomes 17q and 22q, demarcated by the COL1A1 and PDGFbeta genes, respectively, was associated with elevated expression of the amplified genes.
引用
收藏
页码:2383 / 2395
页数:13
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