Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids

Background: Photodynamic therapy (PDT) and radiotherapy using ionizing radiation (IR) are promising options for organ-preserving treatment of bladder cancer (BCa). A combination therapy (IR+PDT) could be beneficial for BCa treatment. Purpose: For PDT, we used the near-infrared photosensitizer tetrah...

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Main Authors: Annabell Reinhold, Annegret Glasow, Sandra Nürnberger, Annett Weimann, Lucie Telemann, Jens-Uwe Stolzenburg, Jochen Neuhaus, Mandy Berndt-Paetz
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:Photodiagnosis and Photodynamic Therapy
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Online Access:http://www.sciencedirect.com/science/article/pii/S1572100024004952
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author Annabell Reinhold
Annegret Glasow
Sandra Nürnberger
Annett Weimann
Lucie Telemann
Jens-Uwe Stolzenburg
Jochen Neuhaus
Mandy Berndt-Paetz
author_facet Annabell Reinhold
Annegret Glasow
Sandra Nürnberger
Annett Weimann
Lucie Telemann
Jens-Uwe Stolzenburg
Jochen Neuhaus
Mandy Berndt-Paetz
author_sort Annabell Reinhold
collection DOAJ
description Background: Photodynamic therapy (PDT) and radiotherapy using ionizing radiation (IR) are promising options for organ-preserving treatment of bladder cancer (BCa). A combination therapy (IR+PDT) could be beneficial for BCa treatment. Purpose: For PDT, we used the near-infrared photosensitizer tetrahydroporphyrin-tetratosylate (THPTS) showing high therapeutic efficacy. Treatment responses were analyzed in BCa organoids. Methods: Organoids consisting of BCa cells lines, bladder fibroblasts and muscle cells were treated with IR (9 Gy) and/or PDT using THPTS (25, 50 μM; 20 J/cm2). Cytotoxicity was determined by microscopy, cell-based assays and histology. The cell death mode was analyzed by applying specific inhibitors followed by immunofluorescence or qPCR analyses of cell death markers. A matrix-based co-culture model was used to study T cell migration into the environment of treated organoids. Results: PDT and/or IR resulted in concentration-dependent reduction of metabolic activity, organoid diameter and integrity. Higher cytotoxicity of IR+PDT vs. monotherapies was observed after 72 h. Non-malignant organoids showed no cytotoxic effects. While apoptosis, necroptosis and ferroptosis were clearly involved in cell death of T-24 cells, cytotoxicity in RT-112 cells was probably provoked by apoptosis, ferroptosis and pyroptosis. IR+PDT resulted in significant migration of Jurkat cells into ECM-embedded organoids within 3 days after treatment. Conclusion: Treatment with IR+PDT showed tumor-selective cytotoxicity with additive or synergistic effects in BCa organoids. Thereby, IR+PDT led to multimodal cell death depending on the cellular context. Migration of T cells into the organoid environment illustrates the immunogenic potential of IR+PDT. Therefore, it might be a promising approach for organ-preserving BCa treatment.
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spelling doaj-art-54412df185a644c0a700d4249b00f5e22025-02-01T04:11:47ZengElsevierPhotodiagnosis and Photodynamic Therapy1572-10002025-02-0151104459Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoidsAnnabell Reinhold0Annegret Glasow1Sandra Nürnberger2Annett Weimann3Lucie Telemann4Jens-Uwe Stolzenburg5Jochen Neuhaus6Mandy Berndt-Paetz7Department of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, 04103 Leipzig, GermanyDepartment of Radiation Therapy, University of Leipzig, Stephanstraße 9a, 04103 Leipzig, GermanyDepartment of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, 04103 Leipzig, GermanyDepartment of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, 04103 Leipzig, GermanyDepartment of Urology, University Hospital Leipzig, Liebigstraße 20, 04103 Leipzig, GermanyDepartment of Urology, University Hospital Leipzig, Liebigstraße 20, 04103 Leipzig, GermanyDepartment of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, 04103 Leipzig, GermanyDepartment of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, 04103 Leipzig, Germany; Corresponding author at: Department of Urology, Research Laboratories, University of Leipzig, Liebigstraße 19, Building C, 04103 Leipzig, Germany.Background: Photodynamic therapy (PDT) and radiotherapy using ionizing radiation (IR) are promising options for organ-preserving treatment of bladder cancer (BCa). A combination therapy (IR+PDT) could be beneficial for BCa treatment. Purpose: For PDT, we used the near-infrared photosensitizer tetrahydroporphyrin-tetratosylate (THPTS) showing high therapeutic efficacy. Treatment responses were analyzed in BCa organoids. Methods: Organoids consisting of BCa cells lines, bladder fibroblasts and muscle cells were treated with IR (9 Gy) and/or PDT using THPTS (25, 50 μM; 20 J/cm2). Cytotoxicity was determined by microscopy, cell-based assays and histology. The cell death mode was analyzed by applying specific inhibitors followed by immunofluorescence or qPCR analyses of cell death markers. A matrix-based co-culture model was used to study T cell migration into the environment of treated organoids. Results: PDT and/or IR resulted in concentration-dependent reduction of metabolic activity, organoid diameter and integrity. Higher cytotoxicity of IR+PDT vs. monotherapies was observed after 72 h. Non-malignant organoids showed no cytotoxic effects. While apoptosis, necroptosis and ferroptosis were clearly involved in cell death of T-24 cells, cytotoxicity in RT-112 cells was probably provoked by apoptosis, ferroptosis and pyroptosis. IR+PDT resulted in significant migration of Jurkat cells into ECM-embedded organoids within 3 days after treatment. Conclusion: Treatment with IR+PDT showed tumor-selective cytotoxicity with additive or synergistic effects in BCa organoids. Thereby, IR+PDT led to multimodal cell death depending on the cellular context. Migration of T cells into the organoid environment illustrates the immunogenic potential of IR+PDT. Therefore, it might be a promising approach for organ-preserving BCa treatment.http://www.sciencedirect.com/science/article/pii/S1572100024004952Photodynamic therapyNear-infrared photosensitizerIonizing radiationBladder cancer organoidsMultimodal, synergistic cytotoxicityImmune cell invasion
spellingShingle Annabell Reinhold
Annegret Glasow
Sandra Nürnberger
Annett Weimann
Lucie Telemann
Jens-Uwe Stolzenburg
Jochen Neuhaus
Mandy Berndt-Paetz
Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
Photodiagnosis and Photodynamic Therapy
Photodynamic therapy
Near-infrared photosensitizer
Ionizing radiation
Bladder cancer organoids
Multimodal, synergistic cytotoxicity
Immune cell invasion
title Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
title_full Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
title_fullStr Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
title_full_unstemmed Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
title_short Ionizing radiation and photodynamic therapy lead to multimodal tumor cell death, synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
title_sort ionizing radiation and photodynamic therapy lead to multimodal tumor cell death synergistic cytotoxicity and immune cell invasion in human bladder cancer organoids
topic Photodynamic therapy
Near-infrared photosensitizer
Ionizing radiation
Bladder cancer organoids
Multimodal, synergistic cytotoxicity
Immune cell invasion
url http://www.sciencedirect.com/science/article/pii/S1572100024004952
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