Standard name |
MYLLYKANGAS_AMPLIFICATION_HOT_SPOT_25 |
Systematic name |
M16082 |
Brief description |
Amplification hot spot 25: colocalized fragile sites and cancer genes in the 2q13-q36 region. |
Full description or abstract |
DNA copy number amplifications activate oncogenes and are hallmarks of nearly all advanced tumors. Amplified genes represent attractive targets for therapy, diagnostics and prognostics. To investigate DNA amplifications in different neoplasms, we performed a bibliomics survey using 838 published chromosomal comparative genomic hybridization studies and collected amplification data at chromosome band resolution from more than 4500 cases. Amplification profiles were determined for 73 distinct neoplasms. Neoplasms were clustered according to the amplification profiles, and frequently amplified chromosomal loci (amplification hot spots) were identified using computational modeling. To investigate the site specificity and mechanisms of gene amplifications, colocalization of amplification hot spots, cancer genes, fragile sites, virus integration sites and gene size cohorts were tested in a statistical framework. Amplification-based clustering demonstrated that cancers with similar etiology, cell-of-origin or topographical location have a tendency to obtain convergent amplification profiles. The identified amplification hot spots were colocalized with the known fragile sites, cancer genes and virus integration sites, but global statistical significance could not be ascertained. Large genes were significantly overrepresented on the fragile sites and the reported amplification hot spots. These findings indicate that amplifications are selected in the cancer tissue environment according to the qualitative traits and localization of cancer genes. |
Collection |
C2: Curated CGP: Chemical and Genetic Perturbations |
Source publication |
Pubmed 16751803 Authors: Myllykangas S,Himberg J,Böhling T,Nagy B,Hollmén J,Knuutila S |
Exact source |
Table 1: 2q13-q36 |
Related gene sets |
(show 20 additional gene sets from the source publication)
(show 2 gene sets from the same authors)
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External links |
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Source species |
Homo sapiens |
Contributed by |
Arthur Liberzon (MSigDB Team) |
Source platform or identifier namespace |
HUMAN_GENE_SYMBOL |
Dataset references |
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NCI-60 cell lines (National Cancer Institute)
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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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these 9 genes
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Gene families ? |
Categorize these
9 genes by gene family
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Show members |
(show 15 source identifiers mapped to 9 genes)
Source Id |
NCBI (Entrez) Gene Id |
Gene Symbol |
Gene Description |
ATIC |
471 |
ATIC |
5-aminoimidazole-4-carboxamide ribonucleotid... |
CHN1 |
1123 |
CHN1 |
chimerin 1 [Source:HGNC Symbol;Acc:HGNC:1943] |
ERCC3 |
2071 |
ERCC3 |
ERCC excision repair 3, TFIIH core complex h... |
FEV |
54738 |
FEV |
FEV transcription factor, ETS family member ... |
FRA2B |
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FRA2F |
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FRA2G |
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FRA2H |
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FRA2I |
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FRA2K |
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HOXD11 |
3237 |
HOXD11 |
homeobox D11 [Source:HGNC Symbol;Acc:HGNC:5134] |
HOXD13 |
3239 |
HOXD13 |
homeobox D13 [Source:HGNC Symbol;Acc:HGNC:5136] |
PAX3 |
5077 |
PAX3 |
paired box 3 [Source:HGNC Symbol;Acc:HGNC:8617] |
PMS1 |
5378 |
PMS1 |
PMS1 homolog 1, mismatch repair system compo... |
TTL |
150465 |
TTL |
tubulin tyrosine ligase [Source:HGNC Symbol;... |
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Version history |
3.0: First introduced
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