Department of Oral and Maxillofacial Surgery, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan
Division of Biochemistry, Meikai University School of Dentistry, Sakado, Japan.
Anticancer Res. 2020 Jul;40(7):3685-3696. doi: 10.21873/anticanres.14357.
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.
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 subG phase) and cells at different stages of cell cycle (G, S and G/M).
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.
Bortezomib-induced neuropathy might be ameliorated by antioxidants.
背景/目的:虽然奥沙利铂、顺铂、紫杉醇和硼替佐米等化疗药物常引起严重的周围神经病变,但很少有研究报道预防这种副作用的有效策略。在这项研究中,我们首先研究了这些药物是否比一组 15 种其他抗癌药物引起更高的神经病变,然后研究了抗氧化剂,如抗坏血酸钠、N-乙酰-L-半胱氨酸和维生素 B12 是否对它们有任何保护作用。
用含神经生长因子的无血清培养基反复覆盖诱导 PC12 细胞分化为神经元细胞。用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法测定 19 种抗癌药物对 4 个人口腔鳞状细胞癌细胞系、3 种正常口腔细胞以及未分化和分化的 PC12 细胞的细胞毒性水平。对凋亡细胞(分布在 subG 期)和处于不同细胞周期(G、S 和 G/M)阶段的细胞进行细胞分选。
所有 19 种抗癌药物对 PC12 的细胞毒性均高于口腔正常细胞。其中,硼替佐米对未分化和分化的 PC12 细胞均显示出最高的细胞毒性,并使它们发生凋亡。抗坏血酸钠和 N-乙酰-L-半胱氨酸,但不是维生素 B12,完全逆转了硼替佐米的细胞毒性。
抗氧化剂可能改善硼替佐米引起的周围神经病变。