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Nature Cell Biology 6, 507–514 (1 June 2004) | doi:10.1038/ncb1131

Functional proteomic screens reveal an essential extracellular role for hsp90|[alpha]| in cancer cell invasiveness

Brenda K. Eustace , Takashi Sakurai , Jean K. Stewart , Dean Yimlamai , Christine Unger , Carol Zehetmeier , Blanca Lain , Claudia Torella , Stefan W. Henning , Gerald Beste , Bradley T. Scroggins , Len Neckers , Leodevico L. Ilag & Daniel G. Jay

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 hsp90α isoform, but not hsp90β, is expressed extracellularly where it interacts with the matrix metalloproteinase 2 (MMP2). Inhibition of extracellular hsp90α decreases both MMP2 activity and invasiveness. This role for extracellular hsp90α in MMP2 activation indicates that cell-impermeant anti-hsp90 drugs might decrease invasiveness without the concerns inherent in inhibiting intracellular hsp90.