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艾氏腹水癌细胞中的多胺及其生物合成酶。二胺对肿瘤多胺模式的改变。

Polyamines and their biosynthetic enzymes in Ehrlich ascites-carcinoma cells. Modification of tumour polyamine pattern by diamines.

作者信息

Kallio A, Pösö H, Guha S K, Jänne J

出版信息

Biochem J. 1977 Jul 15;166(1):89-94. doi: 10.1042/bj1660089.

Abstract
  1. Ehrlich ascites-carcinoma cells contained relatively high concentrations of spermidine and spermine, but the putrescine content of the washed cells was less than 10% of that of higher polyamines. 2. Ascites-tumour cells likewise exhibited high activities of L-ornithine decarboxylase (EC 4.1.1.17), S-adenosyl-L-methionine decarboxylase (EC 4.1.1.50), spermidine synthase (EC 2.5.1.16) and spermine synthase. 3. During the first days after the inoculation, the polyamine pattern of the ascites cells was characterized by a high molar ratio of spermidine to spermine, which markedly decreased on aging of the cells. 4. Various diamines injected into mice bearing ascites cells rapidly and powerfully decreased ornithine decarboxylase activity in the carcinoma cells, apparently through a mechanism that was not a direct inhibition of the enzyme in vitro. Cadaverine (1,5-diaminopentane) and 1,6-diaminohexane were the most potent inhibitors of ornithine decarboxylase among the amines tested. 5. Chronic treatment of the mice with diamines resulted in a virtually complete disappearance of ornithine decarboxylase activity, and after 24h a significant decline in spermidine accumulation. 6. Cadaverine appeared to be an especially suitable compound for use as an inhibitor of the synthesis of higher polyamines, at least in Ehrlich ascites cells, since this diamine also acted as a competitive inhibitor for putrescine in the spermidine synthase reaction without being incorporated into the higher polyamines.
摘要
  1. 艾氏腹水癌细胞含有相对较高浓度的亚精胺和精胺,但洗涤后的细胞中腐胺含量不到高级多胺含量的10%。2. 腹水肿瘤细胞同样表现出较高的L-鸟氨酸脱羧酶(EC 4.1.1.17)、S-腺苷-L-甲硫氨酸脱羧酶(EC 4.1.1.50)、亚精胺合酶(EC 2.5.1.16)和精胺合酶活性。3. 在接种后的头几天,腹水细胞的多胺模式以亚精胺与精胺的高摩尔比为特征,随着细胞老化,该比例显著下降。4. 向携带腹水细胞的小鼠体内注射各种二胺,可迅速且有力地降低癌细胞中的鸟氨酸脱羧酶活性,显然是通过一种并非直接在体外抑制该酶的机制。在测试的胺类中,尸胺(1,5-二氨基戊烷)和1,6-二氨基己烷是鸟氨酸脱羧酶最有效的抑制剂。5. 用二胺对小鼠进行长期治疗导致鸟氨酸脱羧酶活性几乎完全消失,24小时后亚精胺积累显著下降。6. 尸胺似乎是一种特别适合用作高级多胺合成抑制剂的化合物,至少在艾氏腹水细胞中如此,因为这种二胺在亚精胺合酶反应中也作为腐胺的竞争性抑制剂,且不会掺入高级多胺中。

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