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卡尔瓦酸及其类似物对肿瘤细胞中鸟氨酸脱羧酶活性的影响。

Effect of calvatic acid and its analogs on ornithine decarboxylase activity in tumour cells.

作者信息

Brossa O, Gadoni E, Olivero A, Seccia M, Miglietta A, Gabriel L, Gravela E

机构信息

Department of Clinic and Biological Sciences, University of Turin, Italy.

出版信息

Res Commun Chem Pathol Pharmacol. 1990 Nov;70(2):143-53.

PMID:2277863
Abstract

Calvatic acid (p-carboxyphenylazoxycyanide) is an antibiotic containing an azoxycyano group that displays carcinostatic activity. In the present work it has been shown that in AH-130 hepatoma and K562 leukemia cells the antibiotic, at low concentration, decreases ornithine decarboxylase (ODC) levels. The change depends on two summative effects of the drug, impairment of overall protein synthesis and inhibition of enzyme activity. Some analogs of calvatic acid have been tested in order to gain more insight into the structure-activity relationship. The decarboxylated derivative phenylazoxycyanide proved to be more effective in reducing protein synthesis and ODC activity in the whole tumor cells. The rapidly growing K562 cells displayed high sensitivity to this compound. Calvatic acid analogs devoid of the cyano group were less effective on the same parameters.

摘要

卡尔瓦酸(对羧基苯基偶氮氰化物)是一种含有偶氮氰基的抗生素,具有抗癌活性。在目前的研究中发现,在AH - 130肝癌细胞和K562白血病细胞中,低浓度的该抗生素会降低鸟氨酸脱羧酶(ODC)的水平。这种变化取决于药物的两种累加效应,即整体蛋白质合成的受损和酶活性的抑制。为了更深入了解构效关系,对卡尔瓦酸的一些类似物进行了测试。脱羧衍生物苯基偶氮氰化物在降低整个肿瘤细胞中的蛋白质合成和ODC活性方面被证明更有效。快速生长的K562细胞对该化合物表现出高敏感性。不含氰基的卡尔瓦酸类似物在相同参数上效果较差。

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