Enamel matrix derivative is a potent inhibitor of breast cancer cell attachment to bone

被引:6
作者
Takayama, T
Suzuki, N
Narukawa, M
Goldberg, HA
Otsuka, K
Ito, K
机构
[1] Nihon Univ, Dept Biochem, Sch Dent, Chiyoda Ku, Tokyo 1018310, Japan
[2] Nihon Univ, Dept Periodontol, Sch Dent, Chiyoda Ku, Tokyo 1018310, Japan
[3] Nihon Univ, Div Funct Morphol, Sch Dent, Dent Res Ctr, Tokyo 1018310, Japan
[4] Univ Western Ontario, Canadian Inst Hlth Res Grp Skeletal Dev & Remodel, Div Oral Biol & Dev Biochem, London, ON N6A 5C1, Canada
[5] Nihon Univ, Sch Dent, Div Adv Dent Treatment, Dent Res Ctr, Tokyo 1018310, Japan
关键词
enamel matrix derivative; breast cancer; metastasis; bone; bone sialoprotein;
D O I
10.1016/j.lfs.2004.07.025
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
This study examined whether enamel matrix derivative (EMD) inhibits the adhesion of cancer cells to bone. A typical breast cancer cell line, MCF-7, was used. Conditioned human osteosarcoma cell (Saos-2) medium was used as extracellular bone matrix (ECBM) to measure cell attachment. MCF-7 cells were incubated on ECBM-coated culture plates with or without soluble EMD, Arg-Gly-Asp (RGD) sequence blocking peptides, recombinant bone sialoprotein (rBSP), or specific integrin antibodies, and the attached cells were quantified using toluidine blue staining. EMD markedly reduced the attachment of MCF-7 cells to ECBM in a dose-dependent manner. An RGD peptide (GRGDSP) and recombinant BSP inhibited cell attachment to the same degree as EMD. Similarly, anti-alphavbeta3 integrin antibody strongly reduced cell attachment, whereas anti-alphavbeta5 and anti-beta1 integrin antibodies had less marked effects on cell attachment. These results show that EMD inhibits MCF-7 cell attachment to a bone matrix and that it might be useful as an anti-adhesive agent for breast cancer cells to bone in vivo. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1211 / 1221
页数:11
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