Increased radiosensitivity and radiothermosensitivity of human pancreatic MIA PaCa-2 and U251 glioblastoma cell lines treated with the novel Hsp90 inhibitor NVP-HSP990
Autor: | Dušan, Milanović, Elke, Firat, Anca Ligia, Grosu, Gabriele, Niedermann |
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Rok vydání: | 2012 |
Předmět: |
Radiation-Sensitizing Agents
Brain Neoplasms Pyridones Research Cell Cycle Antineoplastic Agents Apoptosis Hyperthermia Induced Flow Cytometry Combined Modality Therapy Radiation Tolerance Colony-Forming Units Assay Radiosensitivity Pyrimidines Gamma Rays Radiothermosensitivity Tumor Cells Cultured Humans HSP90 Heat-Shock Proteins NVP-HSP990 Glioblastoma Cell Proliferation |
Zdroj: | Radiation Oncology (London, England) |
ISSN: | 1748-717X |
Popis: | Background and purpose Heat shock Protein 90 (Hsp90) is a molecular chaperone that folds, stabilizes, and functionally regulates many cellular proteins involved in oncogenic signaling and in the regulation of radiosensitivity. It is upregulated in response to stress such a heat. Hyperthermia is a potent radiosensitizer, but induction of Hsp90 may potentially limit its efficacy. Our aim was to investigate whether the new Hsp90 inhibitor NVP-HSP990 increases radiosensitivity, thermosensitivity and radiothermosensitivity of human tumor cell lines. Material and methods U251 glioblastoma and MIA PaCa-2 pancreatic carcinoma cells were used. To determine clonogenic survival, colony forming assays were performed. Cell viability and proliferation were assesed by Trypan blue staining. Cell cycle and apoptosis analyses were performed by flow cytometry. DAPI staining was used to detect mitotic catastrophe. Results NVP-HSP990 increased the thermosensitivity, radiosensitivity and radio-thermosensitivity of both cell lines in clonogenic assays. 72 hours after irradiation with 4 Gy, a significant reduction in cell number associated with considerable G2/M acumulation and mitotic catastrophe as well as cell death by apoptosis/necrosis was observed. Conclusions Treatment with NVP-HSP990 strongly sensitized U251 and MIA PaCa-2 cells to hyperthermia and ionizing radiation or combination thereof through augmentation of G2/M arrest, mitotic catastrophe and associated apoptosis. |
Databáze: | OpenAIRE |
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