Gene expression patterns define pathways correlated with loss of differentiation in lung adenocarcinomas

被引:18
作者
Creighton, C [1 ]
Hanash, S
Beer, D
机构
[1] Univ Michigan, Bioinformat Program, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Pediat & Communicable Dis, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
关键词
gene expression; lung cancer; differentiation; microarray;
D O I
10.1016/S0014-5793(03)00259-X
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
An analysis of microarray data from 86 lung adenocarcinomas reveals hundreds of genes significantly correlated with tumor cell differentiation. A bioinformatics approach of linking these genes to public information from the Locuslink and KEGG databases yields evidence for a loss of tumor cell differentiation being associated with biological processes of cell division, protein degradation, pyrimidine and purine metabolism, oxidative phosphorylation, glyoxylate and dicarboxylate metabolism, folate biosynthesis, and glutamate metabolism. The increased expression of genes involved in these processes is consistent with increased proliferation and metabolism characteristics of poorly differentiated tumors. The complete results of this analysis are available at http://dot.ped.med.umich.edu: 2000/pub/diff/index.htm. (C) 2003 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:167 / 170
页数:4
相关论文
共 11 条
[1]   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
[2]   Gene-expression profiles predict survival of patients with lung adenocarcinoma [J].
Beer, DG ;
Kardia, SLR ;
Huang, CC ;
Giordano, TJ ;
Levin, AM ;
Misek, DE ;
Lin, L ;
Chen, GA ;
Gharib, TG ;
Thomas, DG ;
Lizyness, ML ;
Kuick, R ;
Hayasaka, S ;
Taylor, JMG ;
Iannettoni, MD ;
Orringer, MB ;
Hanash, S .
NATURE MEDICINE, 2002, 8 (08) :816-824
[3]   Folate status: Effects on pathways of colorectal carcinogenesis [J].
Choi, SW ;
Mason, JB .
JOURNAL OF NUTRITION, 2002, 132 (08) :2413S-2418S
[4]  
HARPOLE DH, 1995, CANCER RES, V55, P51
[5]   Role of antimetabolites of purine and pyrimidine nucleotide metabolism in tumor cell differentiation [J].
Hatse, S ;
De Clercq, E ;
Balzarini, J .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (04) :539-555
[6]   The KEGG databases at GenomeNet [J].
Kanehisa, M ;
Goto, S ;
Kawashima, S ;
Nakaya, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :42-46
[7]   Role and function of the 26S proteasome in proliferation and apoptosis [J].
Naujokat, C ;
Hoffmann, S .
LABORATORY INVESTIGATION, 2002, 82 (08) :965-980
[8]   Microarray analysis reveals a major direct role of DNA copy number alteration in the transcriptional program of human breast tumors [J].
Pollack, JR ;
Sorlie, T ;
Perou, CM ;
Rees, CA ;
Jeffrey, SS ;
Lonning, PE ;
Tibshirani, R ;
Botstein, D ;
Borresen-Dale, AL ;
Brown, PO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12963-12968
[9]   RefSeq and LocusLink: NCBI gene-centered resources [J].
Pruitt, KD ;
Maglott, DR .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :137-140
[10]   Glutamate antagonists limit tumor growth [J].
Rzeski, W ;
Ikonomidou, C ;
Turski, L .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (08) :1195-1200