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5-S-半胱氨酰多巴对肿瘤细胞的毒性机制。过氧化氢作为细胞毒性的介质。

The mechanism of toxicity of 5-S-cysteinyldopa to tumour cells. Hydrogen peroxide as a mediator of cytotoxicity.

作者信息

Ito S, Inoue S, Fujita K

出版信息

Biochem Pharmacol. 1983 Jul 1;32(13):2079-81. doi: 10.1016/0006-2952(83)90429-x.

Abstract

5-S-Cysteinyldopa, a melanin precursor, has been shown to possess selective toxicity to tumour cells in vitro and in vivo. The mechanism of cytotoxicity of the catechol was studied in comparison with L-dopa and 5-S-cysteaminyldopamine. Growth inhibition of human neuroblastoma cell line of YT-nu by 5-S-cysteinyldopa was completely depressed by addition of catalase. Superoxide dismutase and five drugs thought to scavenge hydroxyl radicals or quench singlet oxygen had little effect on the cytotoxicity. Hydrogen peroxide itself was also cytotoxic at low concns. These results indicated that hydrogen peroxide was a mediator of the cytotoxicity of 5-S-cysteinyldopa. It is suggested that reaction of the catechol with cellular superoxide radicals contributes to the production of hydrogen peroxide in addition to autoxidation. Catalase reduced the cytotoxicity of L-dopa by half, while it had no inhibitory effect on the strong cytotoxicity of 5-S-cysteaminyldopamine.

摘要

5-S-半胱氨酰多巴是一种黑色素前体,已被证明在体外和体内对肿瘤细胞具有选择性毒性。与左旋多巴和5-S-半胱氨酰多巴胺相比,研究了儿茶酚的细胞毒性机制。添加过氧化氢酶可完全抑制5-S-半胱氨酰多巴对人神经母细胞瘤YT-nu细胞系的生长抑制作用。超氧化物歧化酶和五种被认为可清除羟基自由基或淬灭单线态氧的药物对细胞毒性影响很小。过氧化氢本身在低浓度时也具有细胞毒性。这些结果表明,过氧化氢是5-S-半胱氨酰多巴细胞毒性的介质。有人提出,除了自氧化作用外,儿茶酚与细胞超氧自由基的反应也有助于过氧化氢的产生。过氧化氢酶可使左旋多巴的细胞毒性降低一半,而对5-S-半胱氨酰多巴胺的强细胞毒性没有抑制作用。

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