Qi Baochang, Yu Tiecheng, Wang Chengxue, Wang Tiejun, Yao Jihang, Zhang Xiaomeng, Deng Pengfei, Xia Yongning, Junger Wolfgang G, Sun Dahui
Division of Orthopedic Traumatology, The First Hospital of Jilin University, NO.71 Xinmin Street, Changchun, 130021, China.
Department of Surgery Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
J Exp Clin Cancer Res. 2016 Oct 3;35(1):161. doi: 10.1186/s13046-016-0437-5.
Osteosarcoma is the most prevalent primary malignant bone tumor, but treatment is difficult and prognosis remains poor. Recently, large-dose chemotherapy has been shown to improve outcome but this approach can cause many side effects. Minimizing the dose of chemotherapeutic drugs and optimizing their curative effects is a current goal in the management of osteosarcoma patients.
In our study, trypan blue dye exclusion assay was performed to investigate the optimal conditions for the sensitization of osteosarcoma U2OS cells. Cellular uptake of the fluorophores Lucifer Yellow CH dilithium salt and Calcein was measured by qualitative and quantitative methods. Human MTX ELISA Kit and MTT assay were used to assess the outcome for osteosarcoma U2OS cells in the present of shock wave and methotrexate. To explore the mechanism, P2X7 receptor in U2OS cells was detected by immunofluorescence and the extracellular ATP levels was detected by ATP assay kit. All data were analyzed using SPSS17.0 statistical software. Comparisons were made with t test between two groups.
Treatment of human osteosarcoma U2OS cells with up to 450 shock wave pulses at 7 kV or up to 200 shock wave pulses at 14 kV had little effect on cell viability. However, this shock wave treatment significantly promoted the uptake of Calcein and Lucifer Yellow CH by osteosarcoma U2OS cells. Importantly, shock wave treatment also significantly enhanced the uptake of the chemotherapy drug methotrexate and increased the rate of methotrexate-induced apoptosis. We found that shock wave treatment increased the extracellular concentration of ATP and that KN62, an inhibitor of P2X7 receptor reduced the capacity methotrexate-induced apoptosis.
Our results suggest that shock wave treatment promotes methotrexate-induced apoptosis by altering cell membrane permeability in a P2X7 receptor-dependent manner. Shock wave treatment may thus represent a possible adjuvant therapy for osteosarcoma.
骨肉瘤是最常见的原发性恶性骨肿瘤,但治疗困难且预后仍然很差。最近,大剂量化疗已被证明可改善治疗效果,但这种方法会引起许多副作用。在骨肉瘤患者的治疗中,尽量减少化疗药物的剂量并优化其疗效是当前的目标。
在我们的研究中,进行了台盼蓝染料排除试验以研究骨肉瘤U2OS细胞致敏的最佳条件。通过定性和定量方法测量荧光团荧光素黄CH二锂盐和钙黄绿素的细胞摄取。使用人MTX ELISA试剂盒和MTT试验评估冲击波和甲氨蝶呤存在下骨肉瘤U2OS细胞的结果。为了探索其机制,通过免疫荧光检测U2OS细胞中的P2X7受体,并通过ATP检测试剂盒检测细胞外ATP水平。所有数据均使用SPSS17.0统计软件进行分析。两组之间采用t检验进行比较。
用7 kV下高达450个冲击波脉冲或14 kV下高达200个冲击波脉冲处理人骨肉瘤U2OS细胞对细胞活力影响很小。然而,这种冲击波处理显著促进了骨肉瘤U2OS细胞对钙黄绿素和荧光素黄CH的摄取。重要的是,冲击波处理还显著增强了化疗药物甲氨蝶呤的摄取,并增加了甲氨蝶呤诱导的凋亡率。我们发现冲击波处理增加了细胞外ATP浓度,并且P2X7受体抑制剂KN62降低了甲氨蝶呤诱导的凋亡能力。
我们的结果表明,冲击波处理通过以P2X7受体依赖性方式改变细胞膜通透性来促进甲氨蝶呤诱导的凋亡。因此,冲击波处理可能是骨肉瘤的一种可能的辅助治疗方法。