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Synergistic Effect of Methionine‐depleting Total Parenteral Nutrition with 5‐Fluorouracil on Human Gastric Cancer: A Randomized Prospective Clinical Trial

机译:消耗蛋氨酸的全胃肠外营养与5-氟尿嘧啶对人胃癌的协同作用:一项随机前瞻性临床试验

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摘要

Methionine‐depleting total parenteral nutrition (Met‐depleting TPN), infusing AO‐90 amino acid solution (lacking both L‐methionine and L‐cysteine) as a sole nitrogen source, showed synergistic effects with 5‐fluorouracil (5‐FU) in tumor‐bearing rats and in clinical trials with gastrointestinal tract cancers. In this study, the effect of Met‐depleting TPN with 5‐FU upon thymidylate synthase (TS) activity was examined, and the histological effect of this treatment on human gastric cancer was evaluated. Fourteen preoperative advanced gastric cancer patients were divided randomly into two groups. Seven cases were given Met‐depleting TPN for 7 days before surgery with continuous intravenous administration of 5‐FU (500 mg/body per day; total 4.0 g/body) (AO‐90 group). The other 7 received conventional L‐methionine‐containing TPN with 5‐FU (control group). All patients underwent gastrectomy without complications due to these treatments. Resected materials were examined for TS kinetics, and the anti‐cancer effect was also assessed histopathologically. The specimens in the AO‐90 group showed marked degeneration of cancer, while almost no effect was seen in the control group. The free TS activity of carcinoma tissue in the AO‐90 group was decreased and the TS inhibition rate was increased in comparison with the control group (P= 0.0165 and P= 0.0243, respectively). Met‐depleting TPN appears to play a role as a biomodulator of 5‐FU in human gastric cancer.
机译:消耗蛋氨酸的总肠外营养(消耗蛋氨酸的TPN),注入AO-90氨基酸溶液(缺少L-蛋氨酸和L-半胱氨酸)作为唯一的氮源,显示与5-氟尿嘧啶(5-FU)协同作用荷瘤大鼠以及胃肠道癌的临床试验。在这项研究中,研究了用5-FU消耗Met的TPN对胸苷酸合酶(TS)活性的影响,并评估了该治疗对人胃癌的组织学作用。 14例术前晚期胃癌患者随机分为两组。 7例患者在手术前7天接受了Met消耗性TPN的治疗,并连续静脉内注射5-FU(每天500 mg /人;总量4.0 g /人)(AO-90组)。其他7例接受常规含5-甲硫氨酸的含L-蛋氨酸的TPN(对照组)。由于这些治疗方法,所有患者均接受了胃切除术而没有并发症。检查切除的材料的TS动力学,并通过组织病理学评估抗癌作用。 AO-90组的标本显示出明显的癌症变性,而对照组几乎没有观察到效果。与对照组相比,AO-90组癌组织的游离TS活性降低,TS抑制率增加(分别为P = 0.0165和P = 0.0243)。 Met耗尽型TPN似乎在人类胃癌中起5-FU生物调节剂的作用。

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