Applicability of coexpression networks analysis to anticancer drug targets discovery

被引:1
作者
Ivliev, A. E. [1 ]
Rudneva, V. A. [1 ]
Sergeeva, M. G. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Belozersky Inst Phys Chem Biol, Moscow 119992, Russia
基金
俄罗斯基础研究基金会;
关键词
drug target discovery; coexpression network analysis; EXPRESSION; GLIOBLASTOMA; CONSERVATION; PROGRESSION; LEUKEMIA; DISEASE; CANCER; TESTS;
D O I
10.1134/S0026893310020184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Identification of proteins that can be therapeutically targeted is an important problem in molecular biology. Transcriptomics approaches such as coexpression network analysis have been previously proposed as tools facilitating drug targets discovery. To assess whether coexpression network analysis is applicable to prediction of novel anticancer drug targets, we compared known targets of 103 antineoplastic drugs with those of 776 drugs irrelevant to cancer in terms of their position in the coexpression network of glioblastoma one of the most malignant human cancer types. Affymetrix GeneChip expression data for 93 glioblastoma-surgery samples were analyzed. We were able to identify coexpression modules associated with such processes as proliferation, immune response, neurotransmission, ATP synthesis, extracellular matrix formation and others. Anticancer drug targets were four-fold over-represented in the coexpression module associated with cell proliferation and mitosis relative to the other modules. Network connectivity of drug targets within the mitotic module was found to be highly correlated with the number of anticancer drugs acting upon them. Our results support the hypothesis that hubs in the mitotic module represent potential anticancer drug targets, and confirm applicability of coexpression network analysis to anticancer drug targets identification.
引用
收藏
页码:326 / 333
页数:8
相关论文
共 33 条
[1]   Estimating the cost of new drug development: Is it really $802 million? [J].
Adams, CP ;
Brantner, VV .
HEALTH AFFAIRS, 2006, 25 (02) :420-428
[2]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[3]   Quantifying the relationship between co-expression, co-regulation and gene function [J].
Allocco, DJ ;
Kohane, IS ;
Butte, AJ .
BMC BIOINFORMATICS, 2004, 5 (1)
[4]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[5]   NCBI GEO: archive for high-throughput functional genomic data [J].
Barrett, Tanya ;
Troup, Dennis B. ;
Wilhite, Stephen E. ;
Ledoux, Pierre ;
Rudnev, Dmitry ;
Evangelista, Carlos ;
Kim, Irene F. ;
Soboleva, Alexandra ;
Tomashevsky, Maxim ;
Marshall, Kimberly A. ;
Phillippy, Katherine H. ;
Sherman, Patti M. ;
Muertter, Rolf N. ;
Edgar, Ron .
NUCLEIC ACIDS RESEARCH, 2009, 37 :D885-D890
[6]   MULTIPLE SIGNIFICANCE TESTS - THE BONFERRONI METHOD .10. [J].
BLAND, JM ;
ALTMAN, DG .
BRITISH MEDICAL JOURNAL, 1995, 310 (6973) :170-170
[7]   Glioblastoma in adults [J].
Brandes, Alba A. ;
Tosoni, Alicia ;
Franceschi, Enrico ;
Reni, Michele ;
Gatta, Gernma ;
Vecht, Charles .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2008, 67 (02) :139-152
[8]   Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networks [J].
Carlson, MRJ ;
Zhang, B ;
Fang, ZX ;
Mischel, PS ;
Horvath, S ;
Nelson, SF .
BMC GENOMICS, 2006, 7 (1)
[9]   Statistical tests for differential expression in cDNA microarray experiments [J].
Cui, XQ ;
Churchill, GA .
GENOME BIOLOGY, 2003, 4 (04)
[10]   DAVID: Database for annotation, visualization, and integrated discovery [J].
Dennis, G ;
Sherman, BT ;
Hosack, DA ;
Yang, J ;
Gao, W ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (09)