Large-scale data integration framework provides a comprehensive view on glioblastoma multiforme

被引:130
作者
Ovaska, Kristian [1 ,2 ]
Laakso, Marko [1 ,2 ]
Haapa-Paananen, Saija [3 ,4 ]
Louhimo, Riku [1 ,2 ]
Chen, Ping [1 ,2 ]
Aittomaki, Viljami [1 ,2 ]
Valo, Erkka [1 ,2 ]
Nunez-Fontarnau, Javier [1 ,2 ]
Rantanen, Ville [1 ,2 ]
Karinen, Sirkku [1 ,2 ]
Nousiainen, Kari [1 ,2 ]
Lahesmaa-Korpinen, Anna-Maria [1 ,2 ]
Miettinen, Minna [1 ,2 ]
Saarinen, Lilli [1 ,2 ]
Kohonen, Pekka [3 ,4 ]
Wu, Jianmin [1 ,2 ]
Westermarck, Jukka [5 ,6 ,7 ,8 ]
Hautaniemi, Sampsa [1 ,2 ]
机构
[1] Univ Helsinki, Inst Biomed, Computat Syst Biol Lab, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Genome Scale Biol Res Program, FIN-00014 Helsinki, Finland
[3] VTT Tech Res Ctr, FI-20521 Turku, Finland
[4] Univ Turku, FI-20521 Turku, Finland
[5] Univ Turku, Turku Ctr Biotechnol, FI-20520 Turku, Finland
[6] Abo Akad Univ, FI-20520 Turku, Finland
[7] Univ Turku, Dept Pathol, FI-20521 Turku, Finland
[8] Turku Univ Hosp, FI-20521 Turku, Finland
基金
芬兰科学院;
关键词
BIOINFORMATICS; PLATFORM; MICRORNA-21; LANDSCAPE; PATHWAYS; BIOLOGY; GLIOMA;
D O I
10.1186/gm186
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Coordinated efforts to collect large-scale data sets provide a basis for systems level understanding of complex diseases. In order to translate these fragmented and heterogeneous data sets into knowledge and medical benefits, advanced computational methods for data analysis, integration and visualization are needed. Methods: We introduce a novel data integration framework, Anduril, for translating fragmented large-scale data into testable predictions. The Anduril framework allows rapid integration of heterogeneous data with state-of-the-art computational methods and existing knowledge in bio-databases. Anduril automatically generates thorough summary reports and a website that shows the most relevant features of each gene at a glance, allows sorting of data based on different parameters, and provides direct links to more detailed data on genes, transcripts or genomic regions. Anduril is open-source; all methods and documentation are freely available. Results: We have integrated multidimensional molecular and clinical data from 338 subjects having glioblastoma multiforme, one of the deadliest and most poorly understood cancers, using Anduril. The central objective of our approach is to identify genetic loci and genes that have significant survival effect. Our results suggest several novel genetic alterations linked to glioblastoma multiforme progression and, more specifically, reveal Moesin as a novel glioblastoma multiforme-associated gene that has a strong survival effect and whose depletion in vitro significantly inhibited cell proliferation. All analysis results are available as a comprehensive website. Conclusions: Our results demonstrate that integrated analysis and visualization of multidimensional and heterogeneous data by Anduril enables drawing conclusions on functional consequences of large-scale molecular data. Many of the identified genetic loci and genes having significant survival effect have not been reported earlier in the context of glioblastoma multiforme. Thus, in addition to generally applicable novel methodology, our results provide several glioblastoma multiforme candidate genes for further studies. Anduril is available at http://csbi.ltdk.helsinki.fi/anduril/ The glioblastoma multiforme analysis results are available at http://csbi.ltdk.helsinki.fi/anduril/tcga-gbm/
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页数:12
相关论文
共 34 条
[1]   Breast cancer molecular signatures as determined by SAGE: correlation with lymph node status [J].
Abba, Martin C. ;
Sun, Hongxia ;
Hawkins, Kathleen A. ;
Drake, Jeffrey A. ;
Hu, Yuhui ;
Nunez, Maria I. ;
Gaddis, Sally ;
Shi, Tao ;
Horvath, Steve ;
Sahin, Aysegul ;
Aldaz, C. Marcelo .
MOLECULAR CANCER RESEARCH, 2007, 5 (09) :881-890
[2]   Primary glioblastomas with and without EGFR amplification: Relationship to genetic alterations and clinicopathological features [J].
Benito, Rafael ;
Gil-Benso, Rosario ;
Quilis, Vicente ;
Perez, Miguel ;
Gregori-Romero, Mariela ;
Roldan, Pedro ;
Gonzalez-Darder, Jose ;
Cerda-Nicolas, Miguel ;
Lopez-Gines, Concha .
NEUROPATHOLOGY, 2010, 30 (04) :392-400
[3]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[4]   The landscape of somatic copy-number alteration across human cancers [J].
Beroukhim, Rameen ;
Mermel, Craig H. ;
Porter, Dale ;
Wei, Guo ;
Raychaudhuri, Soumya ;
Donovan, Jerry ;
Barretina, Jordi ;
Boehm, Jesse S. ;
Dobson, Jennifer ;
Urashima, Mitsuyoshi ;
Mc Henry, Kevin T. ;
Pinchback, Reid M. ;
Ligon, Azra H. ;
Cho, Yoon-Jae ;
Haery, Leila ;
Greulich, Heidi ;
Reich, Michael ;
Winckler, Wendy ;
Lawrence, Michael S. ;
Weir, Barbara A. ;
Tanaka, Kumiko E. ;
Chiang, Derek Y. ;
Bass, Adam J. ;
Loo, Alice ;
Hoffman, Carter ;
Prensner, John ;
Liefeld, Ted ;
Gao, Qing ;
Yecies, Derek ;
Signoretti, Sabina ;
Maher, Elizabeth ;
Kaye, Frederic J. ;
Sasaki, Hidefumi ;
Tepper, Joel E. ;
Fletcher, Jonathan A. ;
Tabernero, Josep ;
Baselga, Jose ;
Tsao, Ming-Sound ;
Demichelis, Francesca ;
Rubin, Mark A. ;
Janne, Pasi A. ;
Daly, Mark J. ;
Nucera, Carmelo ;
Levine, Ross L. ;
Ebert, Benjamin L. ;
Gabriel, Stacey ;
Rustgi, Anil K. ;
Antonescu, Cristina R. ;
Ladanyi, Marc ;
Letai, Anthony .
NATURE, 2010, 463 (7283) :899-905
[5]   Analysis of cell-based RNAi screens [J].
Boutros, Michael ;
Bras, Ligia P. ;
Huber, Wolfgang .
GENOME BIOLOGY, 2006, 7 (07)
[6]   A Network Model of a Cooperative Genetic Landscape in Brain Tumors [J].
Bredel, Markus ;
Scholtens, Denise M. ;
Harsh, Griffith R. ;
Bredel, Claudia ;
Chandler, James P. ;
Renfrow, Jaclyn J. ;
Yadav, Ajay K. ;
Vogel, Hannes ;
Scheck, Adrienne C. ;
Tibshirani, Robert ;
Sikic, Branimir I. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 302 (03) :261-275
[7]   Glioblastoma Subclasses Can Be Defined by Activity among Signal Transduction Pathways and Associated Genomic Alterations [J].
Brennan, Cameron ;
Momota, Hiroyuki ;
Hambardzumyan, Dolores ;
Ozawa, Tatsuya ;
Tandon, Adesh ;
Pedraza, Alicia ;
Holland, Eric .
PLOS ONE, 2009, 4 (11)
[8]   Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data [J].
Carvalho, Benilton ;
Bengtsson, Henrik ;
Speed, Terence P. ;
Irizarry, Rafael A. .
BIOSTATISTICS, 2007, 8 (02) :485-499
[9]   Automated Network Analysis Identifies Core Pathways in Glioblastoma [J].
Cerami, Ethan ;
Demir, Emek ;
Schultz, Nikolaus ;
Taylor, Barry S. ;
Sander, Chris .
PLOS ONE, 2010, 5 (02)
[10]   MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells [J].
Chan, JA ;
Krichevsky, AM ;
Kosik, KS .
CANCER RESEARCH, 2005, 65 (14) :6029-6033