Molecular mechanism of radiosensitizing effect of paclitaxel

Abstract

Background & Objective: Paclitaxel is a radiosensitizer which may stabilize microtubules, block the G2/M phase of the cell cycle and thus modulate the radioresponsiveness of tumor cells. However, its potential molecular mechanisms of radiosensitization have not been well understood yet. This study was to investigate the radiosensitizing effect of paclitaxel on human oral epithelium carcinoma (κB) cell line and to explore the molecular mechanism of radiosensitization. Methods: The survival of κB cells following the treatment with paclitaxel and/or radiation was determined by colonyforming assay. The radiosensitizing effect was evaluated by calculating the sensitizing enhancement ratio (SER) with multi-target single hit model. The cell cycle distribution was analyzed by flow cytometry. Differentially expressed genes related to paclitaxel radiosensitization were screened using human Oligo microarray. Expressions of protein regulating cytokinesis 1 (PRC1) and cyclin B2 genes were confirmed by real-time quantitative PCR. Results: The proliferation of κB cells was significantly inhibited by paclitaxel combined with ionizing radiation. The SERD0 and SERDq were (2.40±1.87) and (12.23 ±2.81) respectively, when the concentration of paclitaxel was 20 nmol/l. After the treatment with paclitaxel in combination with irradiation, the percentage of G1 phase cells decreased from (48.32±2.40)% to (15.73± 7.00)% (P<0.01), and the percentage of G2/M phase cells increased from (13.66±2.16)% to (52.51±5.02)% (P<0.01). In total 176 differentially expressed genes were identified to be re$ated to pac$itaxe$ radiosensitization. Ten genes were found to regulate cell division, two of which were upregulated and eight were down-regulated after the treatment. Moreover, the expression of PRC1 and cyclin B2 was decreased. Conclusion: The radiosensitizing effect of paclitaxel on κB cells may be due to the downregulated expression of PRC1 and cyclin B2, resulting in inhibition of mitotic spindle formation and cell necrosis.