Genes commonly upregulated by hypoxia in human breast cancer cells MCF-7 and MDA-MB-231

被引:56
作者
Bando, H
Toi, M [1 ]
Kitada, K
Koike, M
机构
[1] Tokyo Metropolitan Canc & Infect Dis Ctr, Breast Canc Res Grp, Bunkyo Ku, Tokyo 1130087, Japan
[2] Tokyo Med & Dent Univ, Dept Pathol, Bunkyo Ku, Tokyo 1138519, Japan
[3] Nippon Roche Res Ctr, Genome Sci Dept, Kamakura, Kanagawa 2478530, Japan
关键词
breast cancer; hypoxia; microarray;
D O I
10.1016/S0753-3322(03)00098-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Hypoxia is a stress that causes alterations in signal transduction and gene instability. In the cancer microenvironment, hypoxia plays a significant role in forming a tumor phenotype and tumor progression. We aimed to identify the genes upregulated by hypoxia in human breast cancer cell lines, a hormone-dependent MCF-7 and a hormone-independent MDA-MB-231, using microarray analysis. The. se cells were exposed to two oxygen concentrations such as 21% and 1% in a time-course. Out of 12 625 genes, 26 genes were identified as commonly upregulated in both MCF-7 and MDA-MB-231 cells. Some of these genes were already reported as hypoxia-related, but some of those were identified newly. These commonly upregulated genes between hormone-dependent and hormone-independent cells-would be a clue to study hypoxia-related events and to explore the novel therapeutic targets in human breast cancer. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:333 / 340
页数:8
相关论文
共 42 条
[1]  
Amirkhosravi A, 2002, THROMB HAEMOSTASIS, V87, P930
[2]  
Bates S, 1996, ONCOGENE, V13, P1103
[3]   Expression of the gene encoding the proapoptotic Nip3 protein is induced by hypoxia [J].
Bruick, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :9082-9087
[4]   Prognostic significance of a novel hypoxia-regulated marker, carbonic anhydrase IX, in invasive breast carcinoma [J].
Chia, SK ;
Wykoff, CC ;
Watson, PH ;
Han, C ;
Leek, RD ;
Pastorek, J ;
Gatter, KC ;
Ratcliffe, P ;
Harris, AL .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (16) :3660-3668
[5]   Targeting gene expression to hypoxic tumor cells [J].
Dachs, GU ;
Patterson, AV ;
Firth, JD ;
Ratcliffe, PJ ;
Townsend, KMS ;
Stratford, IJ ;
Harris, AL .
NATURE MEDICINE, 1997, 3 (05) :515-520
[6]   Up-regulation of apoptosis inhibitory protein IAP-2 by hypoxia - HIF-1-independent mechanisms [J].
Dong, Z ;
Venkatachalam, MA ;
Wang, JZ ;
Patel, Y ;
Saikumar, P ;
Semenza, GL ;
Force, T ;
Nishiyama, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (22) :18702-18709
[7]   OXYGEN-REGULATED CONTROL ELEMENTS IN THE PHOSPHOGLYCERATE KINASE-1 AND LACTATE-DEHYDROGENASE-A GENES - SIMILARITIES WITH THE ERYTHROPOIETIN 3' ENHANCER [J].
FIRTH, JD ;
EBERT, BL ;
PUGH, CW ;
RATCLIFFE, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6496-6500
[8]   Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours [J].
Graeber, TG ;
Osmanian, C ;
Jacks, T ;
Housman, DE ;
Koch, CJ ;
Lowe, SW ;
Giaccia, AJ .
NATURE, 1996, 379 (6560) :88-91
[9]   HYPOXIA INDUCES ACCUMULATION OF P53 PROTEIN, BUT ACTIVATION OF A G(1)-PHASE CHECKPOINT BY LOW-OXYGEN CONDITIONS IS INDEPENDENT OF P53 STATUS [J].
GRAEBER, TG ;
PETERSON, JF ;
TSAI, M ;
MONICA, K ;
FORNACE, AJ ;
GIACCIA, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) :6264-6277
[10]  
Gruvberger S, 2001, CANCER RES, V61, P5979