Gene expression arrays in cancer research: methods and applications

被引:54
作者
Brentani, RR
Carraro, DM
Verjovski-Almeida, S
Reis, EM
Neves, EJ
de Souza, SJ
Carvalho, AF
Brentani, H
Reis, LFL
机构
[1] Ludwig Inst Canc Res, Sao Paulo, Brazil
[2] Hosp Canc AC Camargo, Sao Paulo, Brazil
[3] Univ Sao Paulo, Inst Quim, Sao Paulo, Brazil
[4] Univ Sao Paulo, Inst Matemat & Estatist, Sao Paulo, Brazil
[5] Univ Sao Paulo, BIOINFO, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
microarrays; array analyses; gene profiling;
D O I
10.1016/j.critrevonc.2004.12.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
During the last 5 years, the number of papers describing data obtained by microarray technology increased exponentially with about 3000 papers in 2003. Undoubtedly, cancer is by far the disease that received most of the attention as far as the amount of data generated. As array technology is rather new and highly dependent on bioinformatics, mathematics and statistics, a clear understanding of the knowledge and information derived from array-based experiments is not widely appreciated. We shall review herein some of the issues related to the construction of DNA arrays, quantities and heterogeneity of probes and targets, the consequences of the physical characteristics of the probes, data extraction and data analysis as well as the applications of array technology. Our goal is to bring to the general audience, some of the basics of array technology and its possible application in oncology. By discussing some of the basic aspects of the methodology, we hope to stimulate criticism concerning the conclusions proposed by authors, especially in the light of the very low degree of reproducibility already proven when commercially available platforms were compared [1]. Regardless of its pitfalls, it is unquestionable that array technology will have a great impact in the management of cancer and its applications will range from the discovery of new drug targets, new molecular tools for diagnosis and prognosis as well as for a tailored treatment that will take into account the molecular determinants of a given tumor. Hence, we shall also highlight some of the already available and promising applications of array technology on the day-to-day practiceof oncology. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:95 / 105
页数:11
相关论文
共 51 条
[1]  
Baudry D, 2000, CLIN CANCER RES, V6, P3957
[2]  
Bilban Martin, 2002, Current Issues in Molecular Biology, V4, P57
[3]   The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tags [J].
Brentani, H ;
Caballero, OL ;
Camargo, AA ;
da Silva, AM ;
da Silva, WA ;
Neto, ED ;
Grivet, M ;
Gruber, A ;
Guimaraes, PEM ;
Hide, W ;
Iseli, C ;
Jongeneel, CV ;
Kelso, J ;
Nagai, MA ;
Ojopi, EPB ;
Osorio, EC ;
Reis, EMR ;
Riggins, GJ ;
Simpson, AJG ;
de Souza, S ;
Stevenson, BJ ;
Strausberg, RL ;
Tajara, EH ;
Verjovski-Almeida, S ;
Acencion, ML ;
Bengtsono, MH ;
Bettonip, F ;
Bodmerq, WF ;
Brionesr, MRS ;
Camargos, LP ;
Caveneet, W ;
Ceruttiu, JM ;
Coelho Andradev, LE ;
Costa dos Santosn, PC ;
Costaw, MCR ;
da Silvaw, IT ;
Esteciox, MRH ;
Ferreiraw, KS ;
Furnarit, FB ;
Faria, M ;
Galantep, PAF ;
Guimaraesy, GS ;
Holandaw, AJ ;
Kimuraz, ET ;
Leerkesp, MR ;
Xin, LA ;
Macielu, RMB ;
Martinsbb, EAL ;
Massirero, KB ;
Melor, ASA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13418-13423
[4]   EST comparison indicates 38% of human mRNAs contain possible alternative splice forms [J].
Brett, D ;
Hanke, J ;
Lehmann, G ;
Haase, S ;
Delbrück, S ;
Krueger, S ;
Reich, J ;
Bork, P .
FEBS LETTERS, 2000, 474 (01) :83-86
[5]   The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome [J].
Camargo, AA ;
Samaia, HPB ;
Dias-Neto, E ;
Simao, DF ;
Migotto, IA ;
Briones, MRS ;
Costa, FF ;
Nagai, MA ;
Verjovski-Almeida, S ;
Zago, MA ;
Andrade, LEC ;
Carrer, H ;
El-Dorry, HFA ;
Espreafico, EM ;
Habr-Gama, A ;
Giannella-Neto, D ;
Goldman, GH ;
Gruber, A ;
Hackel, C ;
Kimura, ET ;
Maciel, RMB ;
Marie, SKN ;
Martins, EAL ;
Nóbrega, MP ;
Paçó-Larson, ML ;
Pardini, MIMC ;
Pereira, GG ;
Pesquero, JB ;
Rodrigues, V ;
Rogatto, SR ;
da Silva, IDCG ;
Sogayar, MC ;
Sonati, MDF ;
Tajara, EH ;
Valentini, SR ;
Alberto, FL ;
Amaral, MEJ ;
Aneas, I ;
Arnaldi, LAT ;
de Assis, AM ;
Bengtson, MH ;
Bergamo, NA ;
Bombonato, V ;
de Camargo, MER ;
Canevari, RA ;
Carraro, DM ;
Cerutti, JM ;
Corrêa, MLC ;
Corrêa, RFR ;
Costa, MCR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12103-12108
[6]   The alternative transcript of CD79b is overexpressed in B-CLL and inhibits signaling for apoptosis [J].
Cragg, MS ;
Chan, HTC ;
Fox, MD ;
Tutt, A ;
Smith, A ;
Oscier, DG ;
Hamblin, TJ ;
Glennie, MJ .
BLOOD, 2002, 100 (09) :3068-3076
[7]   ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome [J].
Croft, L ;
Schandorff, S ;
Clark, F ;
Burrage, K ;
Arctander, P ;
Mattick, JS .
NATURE GENETICS, 2000, 24 (04) :340-341
[8]   Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags [J].
de Souza, SJ ;
Camargo, AA ;
Briones, MRS ;
Costa, FF ;
Nagai, MA ;
Verjovski-Almeida, S ;
Zago, MA ;
Andrade, LEC ;
Carrer, H ;
El-Dorry, HFA ;
Espreafico, EM ;
Habr-Gama, A ;
Giannella-Neto, D ;
Goldman, GH ;
Gruber, A ;
Hackel, C ;
Kimura, ET ;
Maciel, RMB ;
Marie, SKN ;
Martins, EAL ;
Nóbrega, MP ;
Pacó-Larson, ML ;
Pardini, MIMC ;
Pereira, GG ;
Pesquero, JB ;
Rodrigues, V ;
Rogatto, SR ;
da Silva, IDCG ;
Sogayar, MC ;
Sonati, MD ;
Tajara, EH ;
Valentini, SR ;
Acencio, M ;
Alberto, FL ;
Amaral, MEJ ;
Aneas, I ;
Bengtson, MH ;
Carraro, DM ;
Carvalho, AF ;
Carvalho, LH ;
Cerutti, JM ;
Corrêa, MLC ;
Costa, MCR ;
Curcio, C ;
Gushiken, T ;
Ho, PL ;
Kimura, E ;
Leite, LCC ;
Maia, G ;
Majumder, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (23) :12690-12693
[9]  
Efron E., 1993, INTRO BOOTSTRAP
[10]   Advantages of mRNA amplification for microarray analysis [J].
Feldman, AL ;
Costouros, NG ;
Wang, E ;
Qian, M ;
Marincola, FM ;
Alexander, HR ;
Libutti, SK .
BIOTECHNIQUES, 2002, 33 (04) :906-+