High-Throughput Analysis of HGF-Stimulated Cell Scattering

被引:14
作者
Chan, Grace K. Y. [1 ]
Lutterbach, Bart A. [2 ]
Pan, Bo-Sheng [2 ]
Kariv, Ilona [1 ]
Szewczak, Alexander A. [1 ]
机构
[1] Merck Res Labs, Dept Drug Design & Optimizat Automated Lead Optim, Boston, MA 02115 USA
[2] Merck Res Labs, Dept Canc Biol & Therapeut, Boston, MA 02115 USA
关键词
scatter assay; high-content screening; migration; Met; HGF;
D O I
10.1177/1087057108324497
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Historically, only relatively low-throughput or expensive methods have been available to measure cell migration. Hepatocyte growth factor (HGF) is a ligand for the tyrosine kinase receptor Met that, in addition to mediating proliferation and survival, increases cell motility and metastasis. The authors have developed a high-throughput imaging assay for measuring inhibition of HGF-induced scattering in human HPAF-II pancreatic adenocarcinoma cells. Following treatment with test compounds and HGF for 24 h, cells are labeled with a nuclear stain and imaged at 10x magnification. The proximity of neighboring nuclei is measured, and the distribution of internuclear distances across each field of view is used to calculate the fraction of scattered cells. This method of analysis can be extended to other cell types and signaling pathways and, compared with other membrane-based migration assays Currently available, the assay is significantly lower in cost, is less labor intensive, and provides higher throughput. (Journal of Biomolecular Screening 2008:847-854)
引用
收藏
页码:847 / 854
页数:8
相关论文
共 27 条
[1]   Automated measurement of cell motility and proliferation [J].
Bahnson, A ;
Athanassiou, C ;
Koebler, D ;
Qian, L ;
Shun, T ;
Shields, D ;
Yu, H ;
Wang, H ;
Goff, J ;
Cheng, T ;
Houck, R ;
Cowsert, L .
BMC CELL BIOLOGY, 2005, 6 (1)
[2]   ZD1839 ('Iressa')1,2 as an anticancer agent [J].
Baselga, J ;
Averbuch, SD .
DRUGS, 2000, 60 (Suppl 1) :33-40
[3]   Met, metastasis, motility and more [J].
Birchmeier, C ;
Birchmeier, W ;
Gherardi, E ;
Vande Woude, GF .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (12) :915-925
[4]  
Boyden S, 1962, J EXP MED, V115, P435
[5]   Mesenchymal to epithelial transition in development and disease [J].
Chaffer, Christine L. ;
Thompson, Erik W. ;
Williams, Elizabeth D. .
CELLS TISSUES ORGANS, 2007, 185 (1-3) :7-19
[6]   3D free vibration analysis of cross-ply laminated plates with one pair of opposite edges simply supported [J].
Chen, WQ ;
Lüe, CF .
COMPOSITE STRUCTURES, 2005, 69 (01) :77-87
[7]  
Christensen JG, 2003, CANCER RES, V63, P7345
[8]   MOLECULAR-CLONING OF A NEW TRANSFORMING GENE FROM A CHEMICALLY TRANSFORMED HUMAN CELL-LINE [J].
COOPER, CS ;
PARK, M ;
BLAIR, DG ;
TAINSKY, MA ;
HUEBNER, K ;
CROCE, CM ;
VANDEWOUDE, GF .
NATURE, 1984, 311 (5981) :29-33
[9]   Cancer therapy: can the challenge be MET? [J].
Corso, S ;
Comoglio, PM ;
Giordano, S .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (06) :284-292
[10]  
DIRENZO MF, 1995, CANCER RES, V55, P1129