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Enhancement of Antitumor Activity of Cisplatin on Human Gastric Cancer Cells in vitro and in vivo by Buthionine Sulfoximine

机译:丁硫氨酸磺胺嘧啶在体内外增强顺铂对人胃癌细胞的抗肿瘤活性

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摘要

An attempt was made to evaluate the enhancement of the antitumor activity of cisplatin (DDP) by buthionine sulfoximine (BSO) in vitro and in vivo. In the in vitro study, pre‐treatment with BSO (5, 10 and 25 mM) increased the antitumor activity of DDP against the gastric cancer cell lines MKN‐28 and MKN‐45, whereas BSO alone exhibited only slight antitumor activity (inhibition rate, 20–30%). In the in vivo study, the antitumor effects of DDP against human gastric cancer xenografts St‐15 and SC‐l‐NU in BALB/c nuu mice were enhanced pretreatment with BSO, which was administered intraperitoneally at a dose of 500 mg/kg according to a schedule of qd × 3. BSO alone showed no antitumor effects against these tumors in nude mice. The side effects (assessed in terms of death rate and body weight loss) associated with the maximum tolerated dose of DDP (9 mg/kg) were not increased by BSO pretreatment. As BSO increased the antitumor activity of DDP without a corresponding increment of its toxicity, BSO appears to be a promising agent for further study.
机译:试图评估丁硫氨酸亚砜亚胺(BSO)在体外和体内对顺铂(DDP)抗肿瘤活性的增强作用。在体外研究中,用BSO(5、10和25 mM)预处理可增强DDP对胃癌细胞MKN-28和MKN-45的抗肿瘤活性,而单独的BSO仅表现出轻微的抗肿瘤活性(抑制率) ,20–30%)。在体内研究中,DSO对BALB / c nu / nu小鼠中人胃癌异种移植物St-15和SC-1-NU的抗肿瘤作用增强了BSO的预处理,BSO的腹腔注射剂量为500 mg /根据qd×3的时间表,每公斤体重。单独的BSO对裸鼠没有显示出对这些肿瘤的抗肿瘤作用。 BSO预处理并未增加与DDP最大耐受剂量(9 mg / kg)相关的副作用(根据死亡率和体重减轻进行评估)。由于BSO增加了DDP的抗肿瘤活性而没有相应增加其毒性,因此BSO似乎是有希望进行进一步研究的药物。

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