Molecular analysis of two mammary carcinoma cell lines at the transcriptional level as a model system for progression of breast cancer

被引:46
作者
Schiemann, S
Schwirzke, M
Brünner, N
Weidle, UH [1 ]
机构
[1] Boehringer Mannheim GmbH, D-82372 Penzberg, Germany
[2] Rigshosp, Finsen Lab, DK-2100 Copenhagen, Denmark
关键词
breast cancer; differential gene expression; new mitochondrial transcript; new receptor; tumor progression;
D O I
10.1023/A:1021941203905
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a model system for the identification of genes involved in the progression of human breast cancer, differential gene expression in cell lines MCF-7 and MCF-7(ADR) was investigated. The latter cell line is derived from the former. Cell line MCF-7 is estrogen receptor-positive, vimentin-negative and uninvasive in the Matrigel outgrowth assay and in the nude mouse, while MCF-7(ADR) is estrogen receptor-negative, hormone-resistant, vimentin-positive, invasive in the Matrigel outgrowth assay and in the nude mouse and resistant to adriamycin due to overexpression of glycoprotein gp170. We have shown that tumor progression in this model system is mediated by transcriptional regulation of mitochondria-related genes, proteases, transmembrane receptors and cell cycle-related gene proteins. Among the genes differentially regulated at the transcriptional level in the cell lines MCF-7 and MCF-7(ADR) are a new mitochondrial transcript, mitochondrial creatine kinase, matrix metalloproteinase-1, stromelysin-3, urokinase and its receptor, tissue factor, E-cadherin, epidermal growth factor receptor, transmembrane proteins Mat-8 and progression associated protein (PAP), cyclin E, cyclin-dependent kinase-2 and cell cycle inhibitory proteins p16, p21 and p27. (C) 1998 Rapid Science Ltd.
引用
收藏
页码:129 / 139
页数:11
相关论文
共 48 条
  • [1] GROWTH-FACTORS AND CANCER
    AARONSON, SA
    [J]. SCIENCE, 1991, 254 (5035) : 1146 - 1153
  • [2] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME
    ANDERSON, S
    BANKIER, AT
    BARRELL, BG
    DEBRUIJN, MHL
    COULSON, AR
    DROUIN, J
    EPERON, IC
    NIERLICH, DP
    ROE, BA
    SANGER, F
    SCHREIER, PH
    SMITH, AJH
    STADEN, R
    YOUNG, IG
    [J]. NATURE, 1981, 290 (5806) : 457 - 465
  • [3] CADHERIN EXPRESSION IN CARCINOMAS - ROLE IN THE FORMATION OF CELL-JUNCTIONS AND THE PREVENTION OF INVASIVENESS
    BIRCHMEIER, W
    BEHRENS, J
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1994, 1198 (01): : 11 - 26
  • [4] BLASI F, 1988, Fibrinolysis, V2, P73, DOI 10.1016/0268-9499(88)90370-0
  • [5] Bolon I, 1996, LAB INVEST, V75, P1
  • [6] INSULIN-LIKE GROWTH FACTOR-I ACTIVATES THE INVASION SUPPRESSOR FUNCTION OF E-CADHERIN IN MCF-7 HUMAN MAMMARY-CARCINOMA CELLS IN-VITRO
    BRACKE, ME
    VYNCKE, BM
    BRUYNEEL, EA
    VERMEULEN, SJ
    DEBRUYNE, GK
    VANLAREBEKE, NA
    VLEMINCKX, K
    VANROY, FM
    MAREEL, MM
    [J]. BRITISH JOURNAL OF CANCER, 1993, 68 (02) : 282 - 289
  • [7] Buisson AC, 1996, LAB INVEST, V74, P658
  • [8] PRECISE IDENTIFICATION OF INDIVIDUAL PROMOTERS FOR TRANSCRIPTION OF EACH STRAND OF HUMAN MITOCHONDRIAL-DNA
    CHANG, DD
    CLAYTON, DA
    [J]. CELL, 1984, 36 (03) : 635 - 643
  • [9] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [10] THE INTER-RELATIONSHIPS BETWEEN OVARIAN-INDEPENDENT GROWTH, TUMORIGENICITY, INVASIVENESS AND ANTIOESTROGEN RESISTANCE IN THE MALIGNANT PROGRESSION OF HUMAN-BREAST CANCER
    CLARKE, R
    BRUNNER, N
    THOMPSON, EW
    GLANZ, P
    KATZ, D
    DICKSON, RB
    LIPPMAN, ME
    [J]. JOURNAL OF ENDOCRINOLOGY, 1989, 122 (01) : 331 - 340