Whole genome sequence analysis links chromothripsis to EGFR, MDM2, MDM4, and CDK4 amplification in glioblastoma
Author(s) -
John M. Furgason,
Robert F. Koncar,
Sharon K. Michelhaugh,
Fazlul H. Sarkar,
Sandeep Mittal,
Andrew E. Sloan,
Jill S. BarnholtzSloan,
El Mustapha Bahassi
Publication year - 2015
Publication title -
oncoscience
Language(s) - English
Resource type - Journals
ISSN - 2331-4737
DOI - 10.18632/oncoscience.178
Subject(s) - chromothripsis , cdkn2a , biology , cancer research , genome instability , gene duplication , cancer , genetics , computational biology , gene , dna damage , dna
Findings based on recent advances in next-generation sequence analysis suggest that, in some tumors, a single catastrophic event, termed chromothripsis, results in several simultaneous tumorigenic alterations. Previous studies have suggested that glioblastoma (GBM) may exhibit chromothripsis at a higher rate (39%) than other tumors (9%). Primary glioblastoma is an aggressive form of brain cancer that typically appears suddenly in older adults. With aggressive treatment, the median survival time is only 15 months. Their acute onset and widespread genomic instability indicates that chromothripsis may play a key role in their initiation and progression. GBMs are often characterized by EGFR amplification, CDKN2A and PTEN deletion, although approximately 20% of GBMs harbor additional amplifications in MDM2 or MDM4 with CDK4.
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