Functional proteomic screens reveal an essential extracellular role for hsp90α in cancer cell invasiveness

被引:465
作者
Eustace, BK
Sakurai, T
Stewart, JK
Yimlamai, D
Unger, C
Zehetmeier, C
Lain, B
Torella, C
Henning, SW
Beste, G
Scroggins, BT
Neckers, L
Ilag, LL
Jay, DG [1 ]
机构
[1] Tufts Univ, Sch Med, Dept Physiol, Boston, MA 02111 USA
[2] Xerion Pharmaceut AG, D-81377 Munich, Germany
[3] NCI, Cell & Canc Biol Branch, Rockville, MD 20850 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ncb1131
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tumour cell invasiveness is crucial for cancer metastasis and is not yet understood. Here we describe two functional screens for proteins required for the invasion of fibrosarcoma cells that identified the molecular chaperone heat shock protein 90 (hsp90). The hsp90alpha isoform, but not hsp90beta, is expressed extracellularly where it interacts with the matrix metalloproteinase 2 (MMP2). Inhibition of extracellular hsp90alpha decreases both MMP2 activity and invasiveness. This role for extracellular hsp90alpha in MMP2 activation indicates that cell-impermeant anti-hsp90 drugs might decrease invasiveness without the concerns inherent in inhibiting intracellular hsp90.
引用
收藏
页码:507 / 514
页数:8
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