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Glucocorticoid treatment influences prostate cancer cell growth and the tumor microenvironment via altered glucocorticoid receptor signaling in prostate fibroblasts.
Eigentler, Andrea; Handle, Florian; Schanung, Silvia; Degen, Antonia; Hackl, Hubert; Erb, Holger H H; Fotakis, Georgios; Hoefer, Julia; Ploner, Christian; Jöhrer, Karin; Heidegger, Isabel; Pircher, Andreas; Klotz, Werner; Herold, Manfred; Schäfer, Georg; Culig, Zoran; Puhr, Martin.
Affiliation
  • Eigentler A; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Handle F; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Schanung S; Institute of Pathology, Neuropathology and Molecular Pathology, Medical University of Innsbruck, Innsbruck, Austria.
  • Degen A; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Hackl H; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Erb HHH; Institute of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.
  • Fotakis G; Department of Urology, Faculty of Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
  • Hoefer J; Institute of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.
  • Ploner C; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Jöhrer K; Department of Plastic, Reconstructive and Aesthetic Surgery, Medical University of Innsbruck, Innsbruck, Austria.
  • Heidegger I; Innovacell GesmbH, Mitterweg 25, Innsbruck, Austria.
  • Pircher A; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
  • Klotz W; Department of Internal Medicine V, Medical University of Innsbruck, Innsbruck, Austria.
  • Herold M; Department of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
  • Schäfer G; Department of Internal Medicine II, Medical University of Innsbruck, Innsbruck, Austria.
  • Culig Z; Institute of Pathology, Neuropathology and Molecular Pathology, Medical University of Innsbruck, Innsbruck, Austria.
  • Puhr M; Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
Oncogene ; 43(4): 235-247, 2024 Jan.
Article in En | MEDLINE | ID: mdl-38017134
Despite significant therapeutic advances in recent years, treatment of metastatic prostate cancer (PCa) remains palliative, owing to the inevitable occurrence of drug resistance. There is increasing evidence that epithelial glucocorticoid receptor (GR) signaling and changes in the tumor-microenvironment (TME) play important roles in this process. Since glucocorticoids (GCs) are used as concomitant medications in the course of PCa treatment, it is essential to investigate the impact of GCs on stromal GR signaling in the TME. Therefore, general GR mRNA and protein expression was assessed in radical prostatectomy specimens and metastatic lesions. Elevated stromal GR signaling after GC treatment resulted in altered GR-target gene, soluble protein expression, and in a morphology change of immortalized and primary isolated cancer-associated fibroblasts (CAFs). Subsequently, these changes affected proliferation, colony formation, and 3D-spheroid growth of multiple epithelial PCa cell models. Altered expression of extra-cellular matrix (ECM) and adhesion-related proteins led to an ECM remodeling. Notably, androgen receptor pathway inhibitor treatments did not affect CAF viability. Our findings demonstrate that GC-mediated elevated GR signaling has a major impact on the CAF secretome and the ECM architecture. GC-treated fibroblasts significantly influence epithelial tumor cell growth and must be considered in future therapeutic strategies.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms / Cancer-Associated Fibroblasts Limits: Humans / Male Language: En Journal: Oncogene Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2024 Type: Article Affiliation country: Austria

Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms / Cancer-Associated Fibroblasts Limits: Humans / Male Language: En Journal: Oncogene Journal subject: BIOLOGIA MOLECULAR / NEOPLASIAS Year: 2024 Type: Article Affiliation country: Austria