WEE1 inhibition sensitizes osteosarcoma to radiotherapy

• Published in: BMC cancer 2011-04, Vol.11 (1), p.156-156, Article 156
• Main Authors: PosthumaDeBoer, Jantine, Würdinger, Thomas, Graat, Harm C A, van Beusechem, Victor W, Helder, Marco N, van Royen, Barend J, Kaspers, Gertjan J L
• Format: Article
• Language: English
• Subjects: Apoptosis; Apoptosis - drug effects; Apoptosis - genetics; Apoptosis - radiation effects; Bone Neoplasms - physiopathology; Care and treatment; CDC2 Protein Kinase; Cell Cycle - drug effects; Cell Cycle - genetics; Cell Cycle - physiology; Cell Cycle Proteins - antagonists & inhibitors; Cell Cycle Proteins - genetics; Cell Line, Tumor; Cell Survival - drug effects; Cell Survival - genetics; Cell Survival - radiation effects; Cyclin B - metabolism; Cyclin-Dependent Kinases; DNA Damage - drug effects; DNA Damage - radiation effects; Gamma Rays; Gene Expression Profiling; Health aspects; Humans; Nuclear Proteins - antagonists & inhibitors; Nuclear Proteins - genetics; Osteosarcoma; Osteosarcoma - physiopathology; Phosphorylation - drug effects; Phosphorylation - radiation effects; Physiological aspects; Protein Kinase Inhibitors - pharmacology; Protein kinases; Protein-Tyrosine Kinases - antagonists & inhibitors; Protein-Tyrosine Kinases - genetics; Pyrimidines - pharmacology; Radiation Tolerance - genetics; Radiation-Sensitizing Agents - pharmacology; Radiotherapy
• ISSN: 1471-2407; 1471-2407
• DOI: 10.1186/1471-2407-11-156

The use of radiotherapy in osteosarcoma (OS) is controversial due to its radioresistance. OS patients currently treated with radiotherapy generally are inoperable, have painful skeletal metastases, refuse surgery or have undergone an intralesional resection of the primary tumor. After irradiation-induced DNA damage, OS cells sustain a prolonged G(2) cell cycle checkpoint arrest allowing DNA repair and evasion of cell death. Inhibition of WEE1 kinase leads to abrogation of the G(2) arrest and could sensitize OS cells to irradiation induced cell death. WEE1 expression in OS was investigated by gene-expression data analysis and immunohistochemistry of tumor samples. WEE1 expression in OS cell lines and human osteoblasts was investigated by Western blot. The effect of WEE1 inhibition on the radiosensitivity of OS cells was assessed by cell viability and caspase activation analyses after combination treatment. The presence of DNA damage was visualized using immunofluorescence microscopy. Cell cycle effects were investigated by flow cytometry and WEE1 kinase regulation was analyzed by Western blot. WEE1 expression is found in the majority of tested OS tissue samples. Small molecule drug PD0166285 inhibits WEE1 kinase activity. In the presence of WEE1-inhibitor, irradiated cells fail to repair their damaged DNA, and show higher levels of caspase activation. The inhibition of WEE1 effectively abrogates the irradiation-induced G(2) arrest in OS cells, forcing the cells into premature, catastrophic mitosis, thus enhancing cell death after irradiation treatment. We show that PD0166285, a small molecule WEE1 kinase inhibitor, can abrogate the G(2) checkpoint in OS cells, pushing them into mitotic catastrophe and thus sensitizing OS cells to irradiation-induced cell death. This suggests that WEE1 inhibition may be a promising strategy to enhance the radiotherapy effect in patients with OS.