PDGFRα, PDGFRβ and KIT expression/activation in conventional chondrosarcoma

Authors

  • MS Lagonigro,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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    • MSL and ET contributed equally to this work

  • E Tamborini,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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    • MSL and ET contributed equally to this work

  • T Negri,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • S Staurengo,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • GP Dagrada,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • F Miselli,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • E Gabanti,

    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • A Greco,

    1. Department of Experimental Oncology, and Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • PG Casali,

    1. Department of Medical Oncology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • A Carbone,

    1. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
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  • MA Pierotti,

    1. Department of Experimental Oncology, and Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. IFOM, FIRC (Fondazione Italiana Ricerca Cancro), Institute of Molecular Oncology, Milan, Italy
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    • Senior co-authors

  • S Pilotti

    Corresponding author
    1. Experimental Molecular Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    2. Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy
    • Experimental Molecular Pathology, Department of Pathology, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.
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    • Senior co-authors


Abstract

Chondrosarcomas represent 20% of all primary bone sarcomas, and many studies have attempted to unravel molecular targets for future development of new therapies. The aim of this study was to investigate the expression/activation of PDGFRα, PDGFRβ and KIT receptor tyrosine kinases (RTKs) as potential therapeutic targets in conventional central primary chondrosarcomas (CCS). The expression of PDGFRα, PDGFRβ and KIT RTKs was detected in 16 CCSs using immunohistochemistry (IHC), and their level of expression and activation status were analysed by immunoprecipitation and western blot experiments. PDGFRα, PDGFRβ and KIT cDNAs were screened to verify the presence of activating mutations and the presence of the cognate ligands was analysed by means of RT-PCR. RTK gene amplification was further studied by means of fluorescence in situ hybridization (FISH) analysis. The immunophenotyping and biochemical analyses showed that the CCSs co-expressed PDGFRα and PDGFRβ, with the latter showing definitively greater protein expression and phosphorylation levels. PDGFRβ was expressed but not activated in control healthy joint cartilage, in line with no PDGFB detection. Conversely, the KIT gene product did not seem to play a relevant role. These findings, in the absence of activating mutations or an abnormal genomic profile and the presence of PDGFA and PDGFB expression, are consistent with an autocrine/paracrine loop activation of the corresponding receptors. The CCS gene profile described here offers a rationale for the use of RTK inhibitors alone or in combination with chemotherapy, and supports further investigation of RTKs and their downstream signals. Copyright © 2006 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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