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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Protection of bortezomib-induced neurotoxicity by antioxidants
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Protection of bortezomib-induced neurotoxicity by antioxidants

机译:通过抗氧化剂保护Bortezomib诱导的神经毒性

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Background/Aim: Although chemotherapy agents, such as oxaliplatin, cisplatin, paclitaxel and bortezomib frequently cause severe peripheral neuropathy, very few studies have reported the effective strategy to prevent this side effect. In this study, we first investigated whether these drugs show higher neuropathy compared to a set of 15 other anticancer drugs, and then whether antioxidants, such as sodium ascorbate, N-acetyl-L-cysteine, and vitamin B12 have any protective effect against them. Materials and Methods: Rat PC12 cells were induced to differentiate into neuronal cells by repeated overlay of serum-free medium supplemented with nerve growth factor. The cytotoxic levels of anticancer drugs against four human oral squamous cell carcinoma cell lines, three normal oral cells, and undifferentiated and differentiated PC12 cells were determined by the 3-(4, 5- dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide method. Cells were sorted for apoptotic cells (distributed into subG1 phase) and cells at different stages of cell cycle (G1, S and G2/M). Results: All 19 anticancer drugs showed higher cytotoxicity against PC12 compared to oral normal cells. Among them, bortezomib showed the highest cytotoxicity against both undifferentiated and differentiated PC12 cell and, committed them to undergo apoptosis. Sodium ascorbate and N-acetyl-L-cysteine, but not vitamin B12, completely reversed the cytotoxicity of bortezomib. Conclusion: Bortezomibinduced neuropathy might be ameliorated by antioxidants. ?2020 International Institute of Anticancer Research. All rights reserved.
机译:背景/目的:虽然化疗药物如奥沙利铂,顺铂,紫杉醇和硼齐罗布尔经常引起严重的周围神经病变,但很少有研究报告了预防这种副作用的有效策略。在这项研究中,我们首先研究了与一组其他15个其他抗癌药物相比,这些药物是否显示出更高的神经病变,然后是否抗坏血酸钠,N-乙酰-1-半胱氨酸和维生素B12对它们具有任何保护作用。材料和方法:诱导大鼠PC12细胞通过补充神经生长因子的无血清培养基重复覆盖来分化为神经元细胞。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑鎓测定抗癌药物对四种人口腔鳞状细胞癌细胞系,三种正常口腔细胞和未分化和分化的PC12细胞的细胞毒性水平。溴化物法。将细胞分选用于凋亡细胞(分布到SubG1相)和细胞周期(G1,S和G2 / m)的不同阶段的细胞。结果:与口服正常细胞相比,所有19个抗癌药物对PC12的细胞毒性较高。其中,Bortezomib对未分化和分化的PC12细胞显示最高的细胞毒性,并致力于进行细胞凋亡。抗坏血酸钠和N-乙酰基-1-半胱氨酸,但不是维生素B12,完全逆转了Bortezomib的细胞毒性。结论:抗氧化剂可能会改善硼霉菌的神经病。 ?2020国际抗癌研究所。版权所有。

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