Glioblastoma multiforme;
Oncogenomics;
Genomic amplifications;
Homozygous deletions;
SNP array;
Digital karyotyping;
Copy number alterations;
Whole genome scans;
DNA ARRAYS;
HYBRIDIZATION;
MULTIFORME;
MICROARRAYS;
SUBTYPES;
DISTINCT;
CGH;
D O I:
10.1007/s11060-009-9959-4
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Glioblastoma Multiforme (GBM) is a malignant brain cancer that develops after accumulating genomic DNA damage that often includes gene amplifications and/or deletions. These copy number changes can be a critical step in brain tumor development. To evaluate glioblastoma genomic copy number changes, we determined the genome-wide copy number alterations in 31 GBMs. Illumina Bead Arrays were used to assay 22 GBMs and Digital Karyotyping was used on 8 GBM cell lines and one primary sample. The common amplifications we observed for all 31 samples was GLI/CDK4 (22.6%), MDM2 (12.9%) and PIK3C2B/MDM4 (12.9%). In the 22 GBM tumors, EGFR was amplified in 22.7% of surgical biopsies. The most common homozygously deleted region contained CDKN2A/CDKN2B (p15 and p16) occurring in 29% of cases. This data was compiled and compared to published array CGH studies of 456 cases of GBMs. Pooling our Illumina data with published studies yielded these average amplification rates: EGFR-35.7%, GLI/CDK4-13.4%, MDM2-9.2%, PIK3C2B/MDM4-7.7%, and PDGFRA-7.7%. The CDKN2A/CDKN2B locus was deleted in 46.4% of the combined cases. This study provides a larger assessment of amplifications and deletions in glioblastoma patient populations and shows that several different copy number technologies can produce similar results. The main pathways known to be involved in GBM tumor formation such as p53 control, growth signaling, and cell cycle control are all represented by amplifications or deletions of critical pathway genes. This information is potentially important for formulating targeted therapy in glioblastoma and for planning genomic studies.
机构:
MIT, Dept Biol Engn, Cambridge, MA 02139 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Huang, Paul H.
Cavenee, Webster K.
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机构:
Univ Calif San Diego, Ludwig Inst Canc Res, San Diego Branch, La Jolla, CA 92093 USA
Univ Calif San Diego, Ctr Canc, Dept Med, La Jolla, CA 92093 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Cavenee, Webster K.
Furnari, Frank B.
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机构:
Univ Calif San Diego, Ludwig Inst Canc Res, San Diego Branch, La Jolla, CA 92093 USA
Univ Calif San Diego, Ctr Canc, Dept Med, La Jolla, CA 92093 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Furnari, Frank B.
White, Forest M.
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Dept Biol Engn, Cambridge, MA 02139 USA
MIT, Ctr Canc Res, Cambridge, MA 02139 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
机构:
MIT, Dept Biol Engn, Cambridge, MA 02139 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Huang, Paul H.
Cavenee, Webster K.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Ludwig Inst Canc Res, San Diego Branch, La Jolla, CA 92093 USA
Univ Calif San Diego, Ctr Canc, Dept Med, La Jolla, CA 92093 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Cavenee, Webster K.
Furnari, Frank B.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Ludwig Inst Canc Res, San Diego Branch, La Jolla, CA 92093 USA
Univ Calif San Diego, Ctr Canc, Dept Med, La Jolla, CA 92093 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA
Furnari, Frank B.
White, Forest M.
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Dept Biol Engn, Cambridge, MA 02139 USA
MIT, Ctr Canc Res, Cambridge, MA 02139 USAMIT, Dept Biol Engn, Cambridge, MA 02139 USA