Data and Statistical R Code:
Analysis of Oncogenic Signaling Networks in Glioblastoma: Identification of ASPM as a Novel Target
Horvath, S., Nelson S, Mischel PS
Correspondence: shorvath@mednet.ucla.edu
Method: Weighted Gene Co-Expression Network Analysis ( WGCNA )
Weighted Gene Coexpression Network Analysis
ABSTRACT
Here we provide statistical code and data for the paper:
Horvath S, Zhang B, Carlson M, Lu KV, Zhu S, Felciano RM, Laurance MF, Zhao W, Shu, Q, Lee Y, Scheck AC, Liau LM, Wu H, Geschwind DH, Febbo PG, Kornblum HI, Cloughesy TF, Nelson SF, Mischel PS (2006) “Analysis of Oncogenic Signaling Networks in Glioblastoma Identifies ASPM as a Novel Molecular Target”, PNAS | November 14, 2006 | vol. 103 | no. 46 | 17402-17407
Link to paper: PNAS Webpage
Abstract: Glioblastoma is the most common primary malignant brain tumor of adults and one of the most lethal of all cancers. Patients with this disease have a median survival of 15 months from the time of diagnosis despite surgery, radiation and chemotherapy. New treatment approaches are needed. Recent works suggest that glioblastoma patients may benefit from molecularly targeted therapies. Here, we address the compelling need for identification of new molecular targets. Leveraging global gene expression data from two independent sets of clinical tumor samples (n=55 and n=65), we identify a gene coexpression module in glioblastoma that is also present in breast cancer and significantly overlaps with the “meta-signature” (MS) for undifferentiated cancer. Studies in an isogenic model system demonstrate that this module is downstream of the mutant EGFR receptor, EGFRvIII and that it can be inhibited by the EGFR tyrosine kinase inhibitor Erlotinib. We identify ASPM (abnormal spindle-like microcephaly associated) as a key gene within this module and demonstrate its over-expression in glioblastoma relative to normal brain (or body tissues). Finally, we show that ASPM inhibition by siRNA-mediated knockdown inhibits tumor cell proliferation and neural stem cell proliferation, supporting ASPM as a potential molecular target in glioblastoma. Our weighted gene co-expression network analysis (WGCNA) provides a blueprint for leveraging genomic data to identify key control networks and molecular targets for glioblastoma, and the principle eluted from our work can be applied to other cancers.
Contents
Real Data
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- Detailed Materials And Methods Section (without R code)
Microsoft Word Version
- Detailed Materials And Methods Section (without R code)
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- Brain cancer (GBM) data network analysis. The tutorial shows how we constructed our brain cancer networks in 2 independent datasets and how to relate the 2 networks.
Microsoft Word versionPDF version Datasets (Zipped)
Contents part B (the beginning overlaps with part A)
*) Weighted brain cancer network construction based on *3600* most connected genes
*) Gene significance and intramodular connectivity in data sets I and II
*) Module Eigengene and its relationship to individual genes
*) Regressing survival time on individual gene expression and the module eigengene
Microsoft Word version
PDF version
Datasets (Zipped)
- Brain cancer (GBM) data network analysis. The tutorial shows how we constructed our brain cancer networks in 2 independent datasets and how to relate the 2 networks.
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- Breast Cancer Analysis. This tutorial shows how to map the Affymetrix U133A probe set IDs into Rosetta chip data. Then it uses the resulting breast cancer array data to construct a weighted network.
Microsoft Word version
PDF Version
Datasets (Zipped)
- Breast Cancer Analysis. This tutorial shows how to map the Affymetrix U133A probe set IDs into Rosetta chip data. Then it uses the resulting breast cancer array data to construct a weighted network.
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- Cell Line Validation Data. We used dChip pm-mm normalization on the original Affymmetric Cel files. Rows correspond to probes, columns to microarrays samples.
Dataset (Zipped)
- Cell Line Validation Data. We used dChip pm-mm normalization on the original Affymmetric Cel files. Rows correspond to probes, columns to microarrays samples.
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- dChip and RMA Normalized measurements for all probesets on all samples
Datasets (Zipped)
Clinical data for all samplesDataset (Microsoft Excel)
- dChip and RMA Normalized measurements for all probesets on all samples
Network R functions
A simulated gene co-expression network to illustrate the use of the topological overlap matrix for module detection
Microsoft Word version (recommended)
The second most influential publication in the brain tumor field for the year 2006.
Other material regarding weighted gene co-expression network analysis
Weighted Gene Co-Expression Network Page
The weighted gene co-expression network analysis method is described in Theory Paper 1: Zhang and Horvath (2005)
For a more mathematical description of weighted gene co-expression networks consider Theory Papers: Dong and Horvath (2007, 2008)