The Somatic Genomic Landscape of Glioblastoma
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Bady, 2012, MGMT methylation analysis of glioblastoma on the Infinium methylation BeadChip identifies two distinct CpG regions associated with gene silencing and outcome, yielding a prediction model for comparisons across datasets, tumor grades, and CIMP-status, Acta Neuropathol., 124, 547, 10.1007/s00401-012-1016-2
Bartel, 2004, MicroRNAs: genomics, biogenesis, mechanism, and function, Cell, 116, 281, 10.1016/S0092-8674(04)00045-5
Berger, 2012, Melanoma genome sequencing reveals frequent PREX2 mutations, Nature, 485, 502, 10.1038/nature11071
Beroukhim, 2010, The landscape of somatic copy-number alteration across human cancers, Nature, 463, 899, 10.1038/nature08822
Brennan, 2009, Glioblastoma subclasses can be defined by activity among signal transduction pathways and associated genomic alterations, PLoS ONE, 4, e7752, 10.1371/journal.pone.0007752
Callaghan, 1993, A complete description of the EGF-receptor exon structure: implication in oncogenic activation and domain evolution, Oncogene, 8, 2939
Carter, 2012, Absolute quantification of somatic DNA alterations in human cancer, Nat. Biotechnol., 30, 413, 10.1038/nbt.2203
Chapman, 2011, Improved survival with vemurafenib in melanoma with BRAF V600E mutation, N. Engl. J. Med., 364, 2507, 10.1056/NEJMoa1103782
Chen, 2012, STAR RNA-binding protein Quaking suppresses cancer via stabilization of specific miRNA, Genes Dev., 26, 1459, 10.1101/gad.189001.112
Cho, 2011, Glioblastoma-derived epidermal growth factor receptor carboxyl-terminal deletion mutants are transforming and are sensitive to EGFR-directed therapies, Cancer Res., 71, 7587, 10.1158/0008-5472.CAN-11-0821
Ciriello, 2012, Mutual exclusivity analysis identifies oncogenic network modules, Genome Res., 22, 398, 10.1101/gr.125567.111
Dolecek, 2012, CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005-2009, Neuro-oncol., 14, v1, 10.1093/neuonc/nos218
Dunn, 2012, Emerging insights into the molecular and cellular basis of glioblastoma, Genes Dev., 26, 756, 10.1101/gad.187922.112
Hegi, 2005, MGMT gene silencing and benefit from temozolomide in glioblastoma, N. Engl. J. Med., 352, 997, 10.1056/NEJMoa043331
Hodis, 2012, A landscape of driver mutations in melanoma, Cell, 150, 251, 10.1016/j.cell.2012.06.024
Holmes, 2012, Insulin-like growth factor-binding protein 2-driven glioma progression is prevented by blocking a clinically significant integrin, integrin-linked kinase, and NF-κB network, Proc. Natl. Acad. Sci. USA, 109, 3475, 10.1073/pnas.1120375109
Ichimura, 2009, IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas, Neuro-oncol., 11, 341, 10.1215/15228517-2009-025
Imielinski, 2012, Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing, Cell, 150, 1107, 10.1016/j.cell.2012.08.029
Inda, 2010, Tumor heterogeneity is an active process maintained by a mutant EGFR-induced cytokine circuit in glioblastoma, Genes Dev., 24, 1731, 10.1101/gad.1890510
Kannan, 2012, Whole-exome sequencing identifies ATRX mutation as a key molecular determinant in lower-grade glioma, Oncotarget, 3, 1194, 10.18632/oncotarget.689
Killela, 2013, TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal, Proc. Natl. Acad. Sci. USA, 110, 6021, 10.1073/pnas.1303607110
Krol, 2010, The widespread regulation of microRNA biogenesis, function and decay, Nat. Rev. Genet., 11, 597, 10.1038/nrg2843
Kurahashi, 1995, Isolation and characterization of a novel gene deleted in DiGeorge syndrome, Hum. Mol. Genet., 4, 541, 10.1093/hmg/4.4.541
Kuttler, 2007, Formation of non-random extrachromosomal elements during development, differentiation and oncogenesis, Semin. Cancer Biol., 17, 56, 10.1016/j.semcancer.2006.10.007
Liu, 2012, Frequent ATRX mutations and loss of expression in adult diffuse astrocytic tumors carrying IDH1/IDH2 and TP53 mutations, Acta Neuropathol., 124, 615, 10.1007/s00401-012-1031-3
Lovejoy, 2012, Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway, PLoS Genet., 8, e1002772, 10.1371/journal.pgen.1002772
Mermel, 2011, GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers, Genome Biol., 12, R41, 10.1186/gb-2011-12-4-r41
Noushmehr, 2010, Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma, Cancer Cell, 17, 510, 10.1016/j.ccr.2010.03.017
Ohgaki, 2007, Genetic pathways to primary and secondary glioblastoma, Am. J. Pathol., 170, 1445, 10.2353/ajpath.2007.070011
Ozawa, 2010, PDGFRA gene rearrangements are frequent genetic events in PDGFRA-amplified glioblastomas, Genes Dev., 24, 2205, 10.1101/gad.1972310
Park, 2009, miR-29 miRNAs activate p53 by targeting p85 alpha and CDC42, Nat. Struct. Mol. Biol., 16, 23, 10.1038/nsmb.1533
Phillips, 2006, Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis, Cancer Cell, 9, 157, 10.1016/j.ccr.2006.02.019
Sanborn, 2013, Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons, Cancer Res., 10.1158/0008-5472.CAN-13-0186
Schittenhelm, 2009, Comparative analysis of annexin-1 in neuroepithelial tumors shows altered expression with the grade of malignancy but is not associated with survival, Mod. Pathol., 22, 1600, 10.1038/modpathol.2009.132
Schwartzentruber, 2012, Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma, Nature, 482, 226, 10.1038/nature10833
Shono, 2001, Cyclooxygenase-2 expression in human gliomas: prognostic significance and molecular correlations, Cancer Res., 61, 4375
Singh, 2012, Transforming fusions of FGFR and TACC genes in human glioblastoma, Science, 337, 1231, 10.1126/science.1220834
Snuderl, 2011, Mosaic amplification of multiple receptor tyrosine kinase genes in glioblastoma, Cancer Cell, 20, 810, 10.1016/j.ccr.2011.11.005
Sturm, 2012, Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma, Cancer Cell, 22, 425, 10.1016/j.ccr.2012.08.024
Sumazin, 2011, An extensive microRNA-mediated network of RNA-RNA interactions regulates established oncogenic pathways in glioblastoma, Cell, 147, 370, 10.1016/j.cell.2011.09.041
Szerlip, 2012, Intratumoral heterogeneity of receptor tyrosine kinases EGFR and PDGFRA amplification in glioblastoma defines subpopulations with distinct growth factor response, Proc. Natl. Acad. Sci. USA, 109, 3041, 10.1073/pnas.1114033109
Tay, 2011, Coding-independent regulation of the tumor suppressor PTEN by competing endogenous mRNAs, Cell, 147, 344, 10.1016/j.cell.2011.09.029
2008, Comprehensive genomic characterization defines human glioblastoma genes and core pathways, Nature, 455, 1061, 10.1038/nature07385
2012, Comprehensive genomic characterization of squamous cell lung cancers, Nature, 489, 519, 10.1038/nature11404
2012, Comprehensive molecular characterization of human colon and rectal cancer, Nature, 487, 330, 10.1038/nature11252
2012, Comprehensive molecular portraits of human breast tumours, Nature, 490, 61, 10.1038/nature11412
Varela, 2011, Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma, Nature, 469, 539, 10.1038/nature09639
Verhaak, 2010, Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1, Cancer Cell, 17, 98, 10.1016/j.ccr.2009.12.020
Vivanco, 2012, Differential sensitivity of glioma- versus lung cancer-specific EGFR mutations to EGFR kinase inhibitors, Cancer Discov, 2, 458, 10.1158/2159-8290.CD-11-0284
Wiegand, 2010, ARID1A mutations in endometriosis-associated ovarian carcinomas, N. Engl. J. Med., 363, 1532, 10.1056/NEJMoa1008433
Zheng, 2011, DNA hypermethylation profiles associated with glioma subtypes and EZH2 and IGFBP2 mRNA expression, Neuro-oncol., 13, 280, 10.1093/neuonc/noq190
Zheng, 2013, A survey of intragenic breakpoints in glioblastoma identifies a distinct subset associated with poor survival, Genes Dev., 27, 1462, 10.1101/gad.213686.113
Bass, 2011, Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion, Nat. Genet., 43, 964, 10.1038/ng.936
Bengtsson, H., Simpson, K., Bullard, J.and Hansen, K., (2008). Aroma.affymetrix: A generic framework in R for analyzing small to very large Affymetrix data sets in bounded memory, Tech Report #745, Department of Statistics, University of California, Berkeley, February.
Benjamini, 1995, Controlling the false discovery rate: a practical and powerful approach to multiple testing, J. R. Stat. Soc. Series B Stat, Methodol,, 57, 289, 10.1111/j.2517-6161.1995.tb02031.x
Betel, 2008, The microRNA.org resource: targets and expression, Nucleic Acids Res., 36, D149
Chapman, 2011, Initial genome sequencing and analysis of multiple myeloma, Nature, 471, 467, 10.1038/nature09837
Chen, 2006, Natural selection on human microRNA binding sites inferred from SNP data, Nat. Genet., 38, 1452, 10.1038/ng1910
Chen, 2009, BreakDancer: an algorithm for high-resolution mapping of genomic structural variation, Nat. Methods, 6, 677, 10.1038/nmeth.1363
Costello, 2013, Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation, Nucleic Acids Res., 41, e67, 10.1093/nar/gks1443
DePristo, 2011, A framework for variation discovery and genotyping using next-generation DNA sequencing data, Nat. Genet., 43, 491, 10.1038/ng.806
Fisher, 2011, A scalable, fully automated process for construction of sequence-ready human exome targeted capture libraries, Genome Biol., 12, R1, 10.1186/gb-2011-12-1-r1
Friedman, 2009, Most mammalian mRNAs are conserved targets of microRNAs, Genome Res., 19, 92, 10.1101/gr.082701.108
Getz, 2007, Comment on “The consensus coding sequences of human breast and colorectal cancers”, Science, 317, 1500, 10.1126/science.1138764
Grimson, 2007, MicroRNA targeting specificity in mammals: determinants beyond seed pairing, Mol. Cell, 27, 91, 10.1016/j.molcel.2007.06.017
Korn, 2008, Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs, Nat. Genet., 40, 1253, 10.1038/ng.237
Lawrence, 2013, Mutational heterogeneity in cancer and the search for new cancer-associated genes, Nature, 499, 214, 10.1038/nature12213
Lewis, 2005, Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets, Cell, 120, 15, 10.1016/j.cell.2004.12.035
McCarroll, 2008, Integrated detection and population-genetic analysis of SNPs and copy number variation, Nat. Genet., 40, 1166, 10.1038/ng.238
Stransky, 2011, The mutational landscape of head and neck squamous cell carcinoma, Science, 333, 1157, 10.1126/science.1208130
Venkatraman, 2007, A faster circular binary segmentation algorithm for the analysis of array CGH data, Bioinformatics, 23, 657, 10.1093/bioinformatics/btl646
Wang, 2011, SF3B1 and other novel cancer genes in chronic lymphocytic leukemia, N. Engl. J. Med., 365, 2497, 10.1056/NEJMoa1109016