Gene expression profiling identifies molecular subtypes of gliomas

被引:0
作者
Ruty Shai
Tao Shi
Thomas J Kremen
Steve Horvath
Linda M Liau
Timothy F Cloughesy
Paul S Mischel
Stanley F Nelson
机构
[1] Henry E. Singleton Brain Tumor Program,Department of Human Genetics
[2] UCLA School of Medicine,Department of Biostatistics
[3] Henry E. Singleton Brain Tumor Program,Department of Neurosurgery
[4] UCLA School of Medicine,Department of Neurology
[5] Henry E. Singleton Brain Tumor Program,Department of Pathology and Laboratory Medicine
[6] UCLA School of Medicine,undefined
[7] Henry E. Singleton Brain Tumor Program,undefined
[8] UCLA School of Medicine,undefined
[9] Henry E. Singleton Brain Tumor Program,undefined
[10] UCLA School of Medicine,undefined
来源
Oncogene | 2003年 / 22卷
关键词
glioblastoma; gene expression profiling; microarray; glioma;
D O I
暂无
中图分类号
学科分类号
摘要
Identification of distinct molecular subtypes is a critical challenge for cancer biology. In this study, we used Affymetrix high-density oligonucleotide arrays to identify the global gene expression signatures associated with gliomas of different types and grades. Here, we show that the global transcriptional profiles of gliomas of different types and grades are distinct from each other and from the normal brain. To determine whether our data could be used to uncover molecular subtypes without prior knowledge of pathologic type and grade, we performed K-means clustering analysis and found evidence for three clusters with the aid of multidimensional scaling plots. These clusters corresponded to glioblastomas, lower grade astrocytomas and oligodendrogliomas (P<0.00001). A predictor constructed from the 170 genes that are most differentially expressed between the subsets correctly identified the type and grade of all samples, indicating that a relatively small number of genes can be used to distinguish between these molecular subtypes. These results further define molecular subsets of gliomas which may potentially be used for patient stratification, and suggest potential targets for treatment.
引用
收藏
页码:4918 / 4923
页数:5
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