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Cathepsin S in tumours, regional lymph nodes and sera of patients with lung cancer: relation to prognosis
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  • Regular Article
  • Open access
  • Published: 16 October 2001

Cathepsin S in tumours, regional lymph nodes and sera of patients with lung cancer: relation to prognosis

  • J Kos1,2,
  • A Sekirnik1,
  • G Kopitar1,
  • N Cimerman2,
  • K Kayser3,
  • A Stremmer3,
  • W Fiehn4 &
  • …
  • B Werle3,4 

British Journal of Cancer volume 85, pages 1193–1200 (2001)Cite this article

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Abstract

Cysteine proteinase cathepsin S (Cat S) is expressed mainly in lymphatic tissues and has been characterised as a key enzyme in major histocompatibility complex class II (MHC-II) mediated antigen presentation. Cat S has been measured in tissue cytosols of lung parenchyma, lung tumours and lymph nodes and in sera of patients with lung tumours and of healthy controls, by specific enzyme-linked immunosorbent assay (ELISA). A difference in Cat S level was found between tumour and adjacent control tissue cytosols of 60 lung cancer patients (median 4.3 vs. 2.8 ng mg–1protein). In lymph nodes obtained from 24 patients of the same group, the level of Cat S was significantly higher than in tumours or lung parenchyma (P< 0.001). Additionally, significantly higher levels were found in non-infiltrated than in infiltrated lymph nodes (median 16.6 vs 7.5 ng mg–1protein). Patients with low levels of Cat S in tumours and lung parenchyma exhibited a significantly higher risk of death than those with high levels of Cat S (P= 0.025 – tumours;P= 0.02 – parenchyma). Immunohistochemical analysis (IHA) of lung parenchyma revealed a staining reaction in alveolar type II cells, macrophages and bronchial epithelial cells. In regional lymph node tissue, strong staining of Cat S was found in lymphocytes and histiocytes. Nevertheless, Cat S was detected also in tumour cells, independently of their origin. Our results provide evidence that Cat S may be involved in malignant progression. Its role, however, differs from that of the related Cats B and L and could be associated with the immune response rather than with remodelling of extracellular matrix. © 2001 Cancer Research Campaign http://www.bjcancer.com

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Department of Biochemistry and Molecular Biology, Jožef Stefan Institute, Jamova 39, Ljubljana, SI-1000, Slovenia

    J Kos, A Sekirnik & G Kopitar

  2. R&D Division, Department of Biochemical Research and Drug Design, KRKA d.d., Ljubljana, SI-1000, Slovenia

    J Kos & N Cimerman

  3. Thoraxklinik, GmbH, Heidelberg, D-69126, Germany

    K Kayser, A Stremmer & B Werle

  4. Medizinische Klinik und Poliklinik, Ruprecht Karls University, Zentrallabor, D-68115, Heidelberg, Germany

    W Fiehn & B Werle

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Kos, J., Sekirnik, A., Kopitar, G. et al. Cathepsin S in tumours, regional lymph nodes and sera of patients with lung cancer: relation to prognosis. Br J Cancer 85, 1193–1200 (2001). https://doi.org/10.1054/bjoc.2001.2057

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  • Received: 16 February 2001

  • Revised: 19 June 2001

  • Accepted: 02 July 2001

  • Published: 16 October 2001

  • Issue date: 19 October 2001

  • DOI: https://doi.org/10.1054/bjoc.2001.2057

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Keywords

  • Cathepsin S
  • lung tumours
  • ELISA
  • monoclonal antibody
  • MHC-II
  • immunohistochemistry

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