Screening assay for promigratory/antimigratory compounds

被引:11
作者
Rust, WL [1 ]
Huff, JL [1 ]
Plopper, GE [1 ]
机构
[1] Univ Nevada, Dept Biol Sci, Las Vegas, NV 89154 USA
关键词
migration; cytotoxicity; screening; CAI; tamoxifen;
D O I
10.1006/abio.2000.4510
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Large-scale screening strategies aimed at finding anticancer drugs traditionally focus on identifying cytotoxic compounds that attack actively dividing cells. Because progression to malignancy involves acquisition of an aggressively invasive phenotype in addition to hyperproliferation, simple and effective screening strategies for finding compounds that target the invasive aspects of cancer progression may prove valuable for identifying alternative and preventative cancer therapies, Here, we describe a fluorescence-based automated assay for identifying antimigratory compounds, with the ability to discern cytotoxic from noncytotoxic modes of action. With this assay, we analyzed the effects of two drugs on tumorigenic (MDA-MB-435) and nontumorigenic (MCF-10A) human breast cell lines. We chose to compare carboxyamido-triazole (CAI), an experimental compound shown to inhibit migration of various cell types, with tamoxifen, a common preventative and therapeutic anticancer compound. Our assay demonstrated that both these compounds inhibit migration at sublethal concentrations, Furthermore, CAI was more effective than tamoxifen at inhibiting chemotactic and haptotactic migration of both cell limes at all concentrations tested. (C) 2000 Academic Press.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 37 条
[1]  
Bauer KS, 1999, CLIN CANCER RES, V5, P2324
[2]   A NEW SIMPLIFIED SINGLE-FILTER ASSAY FOR INVITRO EVALUATION OF CHEMOTAXIS OF CR-51-LABELED POLYMORPHONUCLEAR LEUKOCYTES [J].
CAPSONI, F ;
MINONZIO, F ;
ONGARI, AM ;
ZANUSSI, C .
JOURNAL OF IMMUNOLOGICAL METHODS, 1989, 120 (01) :125-131
[3]   TAMOXIFEN AND ITS ACTIVE METABOLITE INHIBIT GROWTH OF ESTROGEN RECEPTOR-NEGATIVE MDA-MB-435 CELLS [J].
CHARLIER, C ;
CHARIOT, A ;
ANTOINE, N ;
MERVILLE, MP ;
GIELEN, J ;
CASTRONOVO, V .
BIOCHEMICAL PHARMACOLOGY, 1995, 49 (03) :351-358
[4]   INTEGRINS AND SIGNAL-TRANSDUCTION PATHWAYS - THE ROAD TAKEN [J].
CLARK, EA ;
BRUGGE, JS .
SCIENCE, 1995, 268 (5208) :233-239
[5]   Rapid fluorescence-based measurement of neutrophil migration in vitro [J].
Frevert, CW ;
Wong, VA ;
Goodman, RB ;
Goodwin, R ;
Martin, TR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 213 (01) :41-52
[6]  
GOLDBERGER A, 1998, TECHNICAL B, V428
[7]  
GREVER MR, 1992, SEMIN ONCOL, V19, P622
[8]  
GROTENDORST GR, 1987, METHOD ENZYMOL, V147, P144
[9]   Sensitizing human cervical cancer cells in vitro to ionizing radiation with interferon β or γ [J].
Grüninger, L ;
Cottin, E ;
Li, YX ;
Noël, A ;
Ozsahin, M ;
Coucke, PA .
RADIATION RESEARCH, 1999, 152 (05) :493-498
[10]  
Guerra-Vladusic FK, 1999, INT J ONCOL, V15, P883