Can anti-migratory drugs be screened in vitro? A review of 2D and 3D assays for the quantitative analysis of cell migration

被引:136
作者
Decaestecker, Christine
Debeir, Olivier
Van Ham, Philippe
Kiss, Robert
机构
[1] Univ Libre Bruxelles, Inst Pharm, Toxicol Lab, B-1050 Brussels, Belgium
[2] Univ Libre Bruxelles, Fac Sci Appl, Dept Log & Numer Syst, Brussels, Belgium
关键词
cell migration; cell invasion; in vitro assay; anti-cancer strategy; anti-migratory drug;
D O I
10.1002/med.20078
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of the present review is to detail and analyze the pros and cons of in vitro tests available to quantify the anti-migratory effects of anti-cancer drugs for their eventual use in combating the dispersal of tumor cells, a clinical need which currently remains unsatisfied. We therefore briefly sum up why anti-migratory drugs constitute a promising approach in oncology while at the same time emphasizing that migrating cancer cells are resistant to apoptosis. To analyze the pros and cons of the various in vitro tests under review we also briefly sum up the molecular and cellular stages of cancer cell migration, an approach that enables us to argue both that no single in vitro test is sufficient to characterize the anti-migratory potential of a drug and that standardization is needed for the efficient quantitative analysis of cell locomotion in a 3D environment. Before concluding our review we devote the final two parts (i) to the description of new prototypes which, in the near future, could enter the screening process with a view to identifying novel anti-migratory compounds, and (ii) to the anti-migratory compounds currently developed against cancer, with particular emphasis on how these compounds were selected before entering the clinical trial phase. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:149 / 176
页数:28
相关论文
共 185 条
[81]   Increased synthesis of hyaluronate enhances motility of human melanoma cells [J].
Ichikawa, T ;
Itano, N ;
Sawai, T ;
Kimata, K ;
Koganehira, Y ;
Saida, T ;
Taniguchi, S .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (06) :935-939
[82]   Integrins: roles in cancer development and as treatment targets [J].
Jin, H ;
Varner, J .
BRITISH JOURNAL OF CANCER, 2004, 90 (03) :561-565
[83]   Microtubules and actin filaments: dynamic targets for cancer chemotherapy [J].
Jordan, MA ;
Wilson, L .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (01) :123-130
[84]   Basement membranes: Structure, assembly and role in tumour angiogenesis [J].
Kalluri, R .
NATURE REVIEWS CANCER, 2003, 3 (06) :422-433
[85]   What's wrong with our cancer models? [J].
Kamb, A .
NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (02) :161-165
[86]   Tumor invasion as dysregulated cell motility [J].
Kassis, J ;
Lauffenburger, DA ;
Turner, T ;
Wells, A .
SEMINARS IN CANCER BIOLOGY, 2001, 11 (02) :105-117
[87]   Electrical wound-healing assay for cells in vitro [J].
Keese, CR ;
Wegener, J ;
Walker, SR ;
Giaever, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (06) :1554-1559
[88]  
Kim YM, 2000, CANCER RES, V60, P5410
[89]   Distinct pathways of cell migration and antiapoptotic response to epithelial injury: Structure-function analysis of human intestinal trefoil factor [J].
Kinoshita, K ;
Taupin, DR ;
Itoh, H ;
Podolsky, DK .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (13) :4680-4690
[90]   Plasminogen activator inhibitor-1 represses integrin- and vitronectin-mediated cell migration independently of its function as an inhibitor of plasminogen activation [J].
Kjoller, L ;
Kanse, SM ;
Kirkegaard, T ;
Rodenburg, KW ;
Ronne, E ;
Goodman, SL ;
Preissner, KT ;
Ossowski, L ;
Andreasen, PA .
EXPERIMENTAL CELL RESEARCH, 1997, 232 (02) :420-429