Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/57896
Title: Cathepsin K induces platelet dysfunction and affects cell signaling in breast cancer - molecularly distinct behavior of cathepsin K in breast cancer
Authors: Andrade, Sheila Siqueira [UNIFESP]
Gouvea, Iuri Estrada [UNIFESP]
Silva, Mariana Cristina C. [UNIFESP]
Castro, Eloisa Dognani [UNIFESP]
de Paula, Claudia A. A. [UNIFESP]
Okamoto, Debora [UNIFESP]
Oliveira, Lilian [UNIFESP]
Peres, Giovani Bravin [UNIFESP]
Ottaiano, Tatiana [UNIFESP]
Facina, Gil [UNIFESP]
Pinto Nazario, Afonso Celso [UNIFESP]
Campos, Antonio Hugo J. F. M.
Paredes-Gamero, Edgar Julian [UNIFESP]
Juliano, Maria [UNIFESP]
da Silva, Ismael D. C. G. [UNIFESP]
Oliva, Maria Luiza V. [UNIFESP]
Girao, Manoel J. B. C. [UNIFESP]
Keywords: Cathepsin K
Platelets
Breast cancer
Protease activated receptors
Issue Date: 2016
Publisher: Biomed Central Ltd
Citation: Bmc Cancer. London, v. 16, p. -, 2016.
Abstract: Background: Breast cancer comprises clinically and molecularly distinct tumor subgroups that differ in cell histology and biology and show divergent clinical phenotypes that impede phase III trials, such as those utilizing cathepsin K inhibitors. Here we correlate the epithelial-mesenchymal-like transition breast cancer cells and cathepsin K secretion with activation and aggregation of platelets. Cathepsin K is up-regulated in cancer cells that proteolyze extracellular matrix and contributes to invasiveness. Although proteolytically activated receptors (PARs) are activated by proteases, the direct interaction of cysteine cathepsins with PARs is poorly understood. In human platelets, PAR-1 and -4 are highly expressed, but PAR-3 shows low expression and unclear functions. Methods: Platelet aggregation was monitored by measuring changes in turbidity. Platelets were immunoblotted with anti-phospho and total p38, Src-Tyr-416, FAK-Tyr-397, and TGF beta monoclonal antibody. Activation was measured in a flow cytometer and calcium mobilization in a confocal microscope. Mammary epithelial cells were prepared from the primary breast cancer samples of 15 women with Luminal-B subtype to produce primary cells. Results: We demonstrate that platelets are aggregated by cathepsin K in a dose-dependent manner, but not by other cysteine cathepsins. PARs-3 and -4 were confirmed as the cathepsin K target by immunodetection and specific antagonists using a fibroblast cell line derived from PARs deficient mice. Moreover, through co-culture experiments, we show that platelets activated by cathepsin K mediated the up-regulation of SHH, PTHrP, OPN, and TGF beta in epithelial-mesenchymal-like cells from patients with Luminal B breast cancer. Conclusions: Cathepsin K induces platelet dysfunction and affects signaling in breast cancer cells.
URI: https://repositorio.unifesp.br/handle/11600/57896
ISSN: 1471-2407
Other Identifiers: http://dx.doi.org/10.1186/s12885-016-2203-7
Appears in Collections:Artigo
Artigo
Artigo

Files in This Item:
File SizeFormat 
WOS000371668400002.pdf3.08 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.