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Expression of FGFR1-4 in Malignant Pleural Mesothelioma Tissue and Corresponding Cell Lines and its Relationship to Patient Survival and FGFR Inhibitor Sensitivity.
Vlacic, Gregor; Hoda, Mir A; Klikovits, Thomas; Sinn, Katharina; Gschwandtner, Elisabeth; Mohorcic, Katja; Schelch, Karin; Pirker, Christine; Peter-Vörösmarty, Barbara; Brankovic, Jelena; Dome, Balazs; Laszlo, Viktoria; Cufer, Tanja; Rozman, Ales; Klepetko, Walter; Grasl-Kraupp, Bettina; Hegedus, Balazs; Berger, Walter; Kern, Izidor; Grusch, Michael.
Afiliação
  • Vlacic G; University Clinic for Respiratory and Allergic Diseases Golnik, 4204 Golnik, Slovenia. gregor.vlacic@klinika-golnik.si.
  • Hoda MA; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. mir.hoda@meduniwien.ac.at.
  • Klikovits T; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. thomas.klikovits@meduniwien.ac.at.
  • Sinn K; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. katharina.sinn@meduniwien.ac.at.
  • Gschwandtner E; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. elisabeth.gschwandtner@meduniwien.ac.at.
  • Mohorcic K; University Clinic for Respiratory and Allergic Diseases Golnik, 4204 Golnik, Slovenia. katja.mohorcic@klinika-golnik.si.
  • Schelch K; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria. karin.schelch@meduniwien.ac.at.
  • Pirker C; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria. christine.pirker@meduniwien.ac.at.
  • Peter-Vörösmarty B; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria. barbara.peter-voeroesmarty@meduniwien.ac.at.
  • Brankovic J; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria. jelena.brankovic@meduniwien.ac.at.
  • Dome B; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. balazs.dome@meduniwien.ac.at.
  • Laszlo V; Department of Tumor Biology, National Koranyi Institute of Pulmonology, 1085 Budapest, Hungary. balazs.dome@meduniwien.ac.at.
  • Cufer T; Department of Thoracic Surgery, National Institute of Oncology-Semmelweis University, 1085 Budapest, Hungary. balazs.dome@meduniwien.ac.at.
  • Rozman A; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. viktoria.laszlo@meduniwien.ac.at.
  • Klepetko W; Department of Tumor Biology, National Koranyi Institute of Pulmonology, 1085 Budapest, Hungary. viktoria.laszlo@meduniwien.ac.at.
  • Grasl-Kraupp B; University Clinic for Respiratory and Allergic Diseases Golnik, 4204 Golnik, Slovenia. tanja.cufer@klinika-golnik.si.
  • Hegedus B; University Clinic for Respiratory and Allergic Diseases Golnik, 4204 Golnik, Slovenia. ales.rozman@klinika-golnik.si.
  • Berger W; Translational Thoracic Oncology Laboratory, Division of Thoracic Surgery, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria. walter.klepetko@meduniwien.ac.at.
  • Kern I; Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, 1090 Vienna, Austria. bettina.grasl-kraupp@meduniwien.ac.at.
  • Grusch M; Department of Thoracic Surgery, University Medicine Essen-Ruhrlandklinik, 45239 Essen, Germany. balazs.hegedues@rlk.uk-essen.de.
Cells ; 8(9)2019 09 16.
Article em En | MEDLINE | ID: mdl-31527449
ABSTRACT
Malignant pleural mesothelioma (MPM) is a devastating malignancy with limited therapeutic options. Fibroblast growth factor receptors (FGFR) and their ligands were shown to contribute to MPM aggressiveness and it was suggested that subgroups of MPM patients could benefit from FGFR-targeted inhibitors. In the current investigation, we determined the expression of all four FGFRs (FGFR1-FGFR4) by immunohistochemistry in tissue samples from 94 MPM patients. From 13 of these patients, we were able to establish stable cell lines, which were subjected to FGFR1-4 staining, transcript analysis by quantitative RT-PCR, and treatment with the FGFR inhibitor infigratinib. While FGFR1 and FGFR2 were widely expressed in MPM tissue and cell lines, FGFR3 and FGFR4 showed more restricted expression. FGFR1 and FGFR2 showed no correlation with clinicopathologic data or patient survival, but presence of FGFR3 in 42% and of FGFR4 in 7% of patients correlated with shorter overall survival. Immunostaining in cell lines was more homogenous than in the corresponding tissue samples. Neither transcript nor protein expression of FGFR1-4 correlated with response to infigratinib treatment in MPM cell lines. We conclude that FGFR3 and FGFR4, but not FGFR1 or FGFR2, have prognostic significance in MPM and that FGFR expression is not sufficient to predict FGFR inhibitor response in MPM cell lines.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Fenilureia / Pirimidinas / Quinazolinas / Acrilamidas / Inibidores de Proteínas Quinases / Neoplasias Pulmonares / Mesotelioma / Antineoplásicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos de Fenilureia / Pirimidinas / Quinazolinas / Acrilamidas / Inibidores de Proteínas Quinases / Neoplasias Pulmonares / Mesotelioma / Antineoplásicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article