Systematic identification and molecular characterization of genes differentially expressed in breast and ovarian cancer

被引:56
作者
Dahl, E
Sadr-Nabavi, A
Klopocki, E
Betz, B
Grube, S
Kreutzfeld, R
Himmelfarb, M
An, HX
Gelling, S
Klaman, I
Hinzmann, B
Kristiansen, G
Grützmann, R
Kuner, R
Petschke, B
Rhiem, K
Wiechen, K
Sers, C
Wiestler, O
Schneider, A
Höfler, H
Nährig, J
Dietel, M
Schäfer, R
Rosenthal, A
Schmutzler, R
Dürst, M
Meindl, A
Niederacher, D
机构
[1] Rhein Westfal TH Aachen, Inst Pathol, D-52074 Aachen, Germany
[2] Ludwig Maximilians Univ Munchen, Dept Pediat, Munich, Germany
[3] MetaGen Pharmaceut IL, Berlin, Germany
[4] Univ Dusseldorf, Dept Obstet & Gynecol, D-4000 Dusseldorf, Germany
[5] Univ Jena, Dept Gynecol, D-6900 Jena, Germany
[6] Univ Cologne, Ctr Med, Dept Gynecol, D-5000 Cologne 41, Germany
[7] Humboldt Univ, Univ Hosp Charite, Inst Pathol, Berlin, Germany
[8] Tech Univ Dresden, Univ Hosp, Dept Visceral Thorac & Vasc Surg, Dresden, Germany
[9] Univ Bonn, Dept Neuropathol, D-5300 Bonn, Germany
[10] Tech Univ Munich, Inst Pathol, D-8000 Munich, Germany
关键词
breast cancer; ovarian cancer; electronic Northern; differentially expressed gene;
D O I
10.1002/path.1687
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The identification of novel disease-associated genes in gynaecological tumours has important for understanding the process of tumourigenesis and the development of novel treatment regimens. cDNA libraries from disease tissues may represent a valuable source to identify such genes. Recently, a bio-informatic procedure based on an 'electronic Northern' approach was established to screen expressed sequence tag (EST) libraries for genes differentially expressed in tumour and normal tissues, and identified 450 candidate genes differentially expressed in breast and ovarian cancer. In this report, the validation of an initial set of 40 candidate genes, which were selected due to their localization in chromosomal regions frequently altered in gynaecological tumours, is described. Differential expression of 29 of these genes, including three uncharacterized novel genes, was confirmed by applying cancer profiling arrays with 106 matched pairs of tumour/normal cDNAs and quantitative reverse transcription-polymerase chain reaction (RT-PCR) on 60 clinical specimens. The majority of these differentially expressed genes have not been described previously in the context of breast and ovarian cancer, and may constitute novel diagnostic markers for these tumour entities. Copyright (C) 2004 Pathological Society of Great Britain and Ireland. Published by John Wiley Sons, Ltd.
引用
收藏
页码:21 / 28
页数:8
相关论文
共 28 条
[1]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[2]   The genetics and genomics of cancer [J].
Balmain, A ;
Gray, J ;
Ponder, B .
NATURE GENETICS, 2003, 33 (Suppl 3) :238-244
[3]   Tensin1 and a previously undocumented family member, tensin2, positively regulate cell migration [J].
Chen, HY ;
Duncan, IC ;
Bozorgchami, H ;
Lo, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :733-738
[4]  
Dong Y, 2002, CANCER RES, V62, P708
[5]   Systematic isolation of genes differentially expressed in normal and cancerous tissue of the pancreas [J].
Grützmann, R ;
Pilarsky, C ;
Staub, E ;
Schmitt, AO ;
Foerder, M ;
Specht, T ;
Hinzmann, B ;
Dahl, E ;
Alldinger, I ;
Rosenthal, A ;
Ockert, D ;
Saeger, HD .
PANCREATOLOGY, 2003, 3 (02) :169-178
[6]   Exploring root symbiotic programs in the model legume Medicago truncatula using EST analysis [J].
Journet, EP ;
van Tuinen, D ;
Gouzy, J ;
Crespeau, H ;
Carreau, V ;
Farmer, MJ ;
Niebel, A ;
Schiex, T ;
Jaillon, O ;
Chatagnier, O ;
Godiard, L ;
Micheli, F ;
Kahn, D ;
Gianinazzi-Pearson, V ;
Gamas, P .
NUCLEIC ACIDS RESEARCH, 2002, 30 (24) :5579-5592
[7]   Caveolin-1 is down-regulated in human ovarian carcinoma and acts as a candidate tumor suppressor gene [J].
Kai, WC ;
Diatchenko, L ;
Agoulnik, A ;
Scharff, KM ;
Schober, H ;
Arlt, K ;
Zhumabayeva, B ;
Siebert, PD ;
Dietel, M ;
Schäfer, R ;
Sers, C .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (05) :1635-1643
[8]   Caspase-dependent cleavage of tensin induces disruption of actin cytoskeleton during apoptosis [J].
Kook, S ;
Kim, DH ;
Shim, SR ;
Kim, W ;
Chun, JS ;
Song, WK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (01) :37-45
[9]   Functions of gelsolin: motility, signaling, apoptosis, cancer [J].
Kwiatkowski, DJ .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (01) :103-108
[10]  
LAI A, 1999, CANCER RES, V59, P5403