Molecular analysis of glioblastoma - Pathway profiling and its implications for patient therapy

被引:47
作者
Mischel, PS
Nelson, SF
Cloughesy, TF
机构
[1] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Human Genet, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Neurol, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Henry E Singleton Brain Canc Res Program, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
glioblastoma; molecular analysis; phosphatidylinositol 3-kinase (PI3K); PTEN; signal transduction; microarray; gene expressionprofiling;
D O I
10.4161/cbt.2.3.369
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Technological advances in the ability to analyze patterns of gene expression and signal transduction pathway activation are improving our understanding of cancer. Previously unrecognized molecular subsets and pathway profiles that convey predictive and prognostic information about individual cancer patients are being identified. Patients with glioblastoma, the most common malignant primary brain tumor of adults, stand to benefit considerably from these advances. Recent data suggest that morphologically indistinguishable glioblastomas have distinct classes of causal oncogene activation, and that these subclasses may be targetable by oncogene/signaling pathway specific therapies. Oncogene/signaling pathway inhibitors show great promise for the treatment of patients with some types of cancer, but their clinical application for glioblastoma has been severely limited by an inability to determine which inhibitor is most likely to benefit a specific patient. Identifying biologically relevant molecular subsets of glioblastoma and detecting pathway profiles that can be used to guide patient therapy are likely to result in significant improvement in the survival of glioblastoma patients.
引用
收藏
页码:242 / 247
页数:6
相关论文
共 41 条
[1]   Towards a novel classification of human malignancies based on gene expression patterns [J].
Alizadeh, AA ;
Ross, DT ;
Perou, CM ;
van de Rijn, M .
JOURNAL OF PATHOLOGY, 2001, 195 (01) :41-52
[2]   Influence of unrecognized molecular heterogeneity on randomized clinical trials [J].
Betensky, RA ;
Louis, DN ;
Cairncross, JG .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (10) :2495-2499
[3]   Oncogenic kinase signalling [J].
Blume-Jensen, P ;
Hunter, T .
NATURE, 2001, 411 (6835) :355-365
[4]  
CHOE G, 2003, IN PRESS CANC RES, P63
[5]   Perspectives on the development of a molecularly targeted agent [J].
Druker, BJ .
CANCER CELL, 2002, 1 (01) :31-36
[6]  
Ermoian RP, 2002, CLIN CANCER RES, V8, P1100
[7]   Signal transduction pathways and their relevance in human astrocytomas [J].
Feldkamp, MM ;
Lau, N ;
Guha, A .
JOURNAL OF NEURO-ONCOLOGY, 1997, 35 (03) :223-248
[8]  
Frederick L, 2000, CANCER RES, V60, P1383
[9]  
Fuller GN, 1999, CANCER RES, V59, P4228
[10]  
Fuller GN, 2002, BRAIN PATHOL, V12, P108