Differential effects of EGF gradient profiles on MDA-MB-231 breast cancer cell chemotaxis

被引:213
作者
Wang, SJ [1 ]
Saadi, W [1 ]
Lin, F [1 ]
Nguyen, CMC [1 ]
Jeon, NL [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92612 USA
关键词
breast cancer; chemotaxis; EGF; migration; gradient profile; microfluidics;
D O I
10.1016/j.yexcr.2004.06.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotaxis, directed cell migration in a gradient of chemoattractant, is an important biological phenomenon that plays pivotal roles in cancer metastasis. Newly developed microfluidic chemotaxis chambers (MCC) were used to study chemotaxis of metastatic breast cancer cells, MDA-MB-231, in EGF gradients of well-defined profiles. Migration behaviors of MDA-MB-231 cells in uniform concentrations of EGF (0, 25, 50, and 100 ng/ml) and EGF (0-25, 0-50, and 0-100 ng/ml) with linear and nonlinear polynomial profiles were investigated. MDA-MB-231 cells exhibited increased speed and directionality upon stimulation with uniform concentrations of EGF. The cells were viable and motile for over 24 h, confirming the compatibility of MCC with cancer cells. Linear concentration gradients of different ranges were not effective in inducing chemotactic movement as compared to nonlinear gradients. MDA-MB-231 cells migrating in EGF gradient of 0-50 ng/ml nonlinear polynomial profile exhibited marked directional movement toward higher EGF concentration. This result suggests that MDA-MB-231 cancer cell chemotaxis depends on the shape of gradient profile as well as on the range of EGF concentrations. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:180 / 189
页数:10
相关论文
共 36 条
  • [1] Epidermal growth factor receptor distribution during chemotactic responses
    Bailly, M
    Wyckoff, J
    Bouzahzah, B
    Hammerman, R
    Sylvestre, V
    Cammer, M
    Pestell, R
    Segall, JE
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (11) : 3873 - 3883
  • [2] Regulation of protrusion shape and adhesion to the substratum during chemotactic responses of mammalian carcinoma cells
    Bailly, M
    Yan, L
    Whitesides, GM
    Condeelis, JS
    Segall, JE
    [J]. EXPERIMENTAL CELL RESEARCH, 1998, 241 (02) : 285 - 299
  • [3] Bailly M, 1998, MICROSC RES TECHNIQ, V43, P433, DOI 10.1002/(SICI)1097-0029(19981201)43:5<433::AID-JEMT9>3.0.CO
  • [4] 2-2
  • [5] Dissemination and growth of cancer cells in metastatic sites
    Chambers, AF
    Groom, AC
    MacDonald, IC
    [J]. NATURE REVIEWS CANCER, 2002, 2 (08) : 563 - 572
  • [6] Intravital imaging of cell movement in tumours
    Condeelis, J
    Segall, JE
    [J]. NATURE REVIEWS CANCER, 2003, 3 (12) : 921 - 930
  • [7] Lamellipodia in invasion
    Condeelis, JS
    Wyckoff, JB
    Bailly, M
    Pestell, R
    Lawrence, D
    Backer, J
    Segall, JE
    [J]. SEMINARS IN CANCER BIOLOGY, 2001, 11 (02) : 119 - 128
  • [8] MAXIMAL MIGRATION OF HUMAN SMOOTH-MUSCLE CELLS ON FIBRONECTIN AND TYPE-IV COLLAGEN OCCURS AT AN INTERMEDIATE ATTACHMENT STRENGTH
    DIMILLA, PA
    STONE, JA
    QUINN, JA
    ALBELDA, SM
    LAUFFENBURGER, DA
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 122 (03) : 729 - 737
  • [9] Multistep navigation and the combinatorial control of leukocyte chemotaxis
    Foxman, EF
    Campbell, JJ
    Butcher, EC
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 139 (05) : 1349 - 1360
  • [10] Temporal and spatial regulation of chemotaxis
    Iijima, M
    Huang, YE
    Devreotes, P
    [J]. DEVELOPMENTAL CELL, 2002, 3 (04) : 469 - 478