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Proteolysis of cystatin C by cathepsin D in the breast cancer microenvironment

In English

Författare

  • Valerie Laurent-Matha
  • Pitter F. Huesgen
  • Olivier Masson
  • Danielle Derocq
  • Christine Prebois
  • Magali Gary-Bobo
  • Fabien Lecaille
  • Bertrand Rebiere
  • Guillaume Meurice
  • Cedric Orear
  • Robert E. Hollingsworth
  • Magnus Abrahamson
  • Gilles Lalmanach
  • Christopher M. Overall
  • Emmanuelle Liaudet-Coopman
Visa allt

Summary, in English

The aspartic protease cathepsin D, a poor prognostic indicator of breast cancer, is abundantly secreted as procathepsin D by human breast cancer cells and self-activates at low pH in vitro, giving rise to catalytically active cathepsin D. Due to a lower extracellular pH in tumor microenvironments compared to normal tissues, cathepsin D may cleave pathophysiological substrates contributing to cancer progression. Here, we show by yeast 2-hybrid and degradomics analyses that cystatin C, the most potent natural secreted inhibitor of cysteine cathepsins, both binds to and is a substrate of extracellular procathepsin D. The amount of cystatin C in the extracellular environment is reduced in the secretome of mouse embryonic fibroblasts stably transfected with human cathepsin D. Cathepsin D extensively cleaved cystatin C in vitro at low pH. Cathepsin D secreted by breast cancer cells also processed cystatin C at the pericellular pH of tumors and so enhancing extracellular proteolytic activity of cysteine cathepsins. Thus, tumor derived cathepsin D assists breast cancer progression by reducing cystatin C activity, which, in turn, enhances cysteine cathepsin proteolytic activity, revealing a new link between protease classes in the protease web.-Laurent-Matha, V., Huesgen, P. F., Masson, O., Derocq, D., Prebois, C., Gary-Bobo, M., Lecaille, F., Rebiere, B., Meurice, G., Orear, C., Hollingsworth, R. E., Abrahamson, M., Lalmanach, G., Overall, C. M., Liaudet-Coopman, E. Proteolysis of cystatin C by cathepsin D in the breast cancer microenvironment. FASEB J. 26, 5172-5181 (2012). www.fasebj.org

Publiceringsår

2012

Språk

Engelska

Sidor

5172-5181

Publikation/Tidskrift/Serie

FASEB Journal

Volym

26

Issue

12

Dokumenttyp

Artikel i tidskrift

Förlag

The Federation of American Societies for Experimental Biology

Ämne

  • Cell and Molecular Biology

Nyckelord

  • cancer
  • protease web

Status

Published

Forskningsgrupp

  • Protease Inhibitor Research

ISBN/ISSN/Övrigt

  • ISSN: 1530-6860