Suppr超能文献

抗肿瘤药物2,2'-(亚甲基二亚氨基)双-1,3,4-噻二唑(NSC 143019)的作用机制

Mechanism of action of 2,2'-(methylenediimino)bis-1,3,4-thiadiazole (NSC 143019), an antitumor agent.

作者信息

Tsukamoto K, Suno M, Igarashi K, Kozai Y, Sugino Y

出版信息

Cancer Res. 1975 Oct;35(10):2631-6.

PMID:125625
Abstract

The mechanism of action of 2,2'-(methylenediimino)bis-1,3,4-thiadiazole (NSC 143019) was clarified by studies on its effects on monolayer cultures of growing cells of the mouse cell line BALB/3T3. At concentrations below 50 muM, NSC 143019 specifically inhibited DNA and RNA syntheses without appreciably affecting protein synthesis. The syntheses of DNA and RNA were inhibited equally and concomitantly by the compound. The inhibition was reversed by removal of the compound and was prevented competitively by an equimolar amount of nicotinamide. It was also reversed completely by guanosine (0.1 mM) or deoxyguanosine (0.1 mM) and was reversed partially by xanthosine (1 mM). Other nucleosides did not influence the inhibition. The inhibition of DNA synthesis by NSC 143019 was not due to inhibition of RNA synthesis, and vice-versa. NSC 143019 inhibited the conversion of [8-14C]hypoxanthine to acid-soluble and -insoluble guanine nucleotides but not to adenine nucleotides. It was strongly suggested from these results that at concentrations of NSC 143019 below 50 muM the primary action of this compound might be due to the inhibition of GMP biosynthesis at the step of conversion of IMP to xanthosine 5'-phosphate.

摘要

通过对2,2'-(亚甲基二亚氨基)双-1,3,4-噻二唑(NSC 143019)对小鼠细胞系BALB/3T3生长细胞单层培养物影响的研究,阐明了其作用机制。在浓度低于50μM时,NSC 143019特异性抑制DNA和RNA合成,而对蛋白质合成无明显影响。该化合物同时且同等程度地抑制DNA和RNA合成。去除该化合物后抑制作用可逆转,等摩尔量的烟酰胺可竞争性阻止这种抑制。鸟苷(0.1 mM)或脱氧鸟苷(0.1 mM)也可使其完全逆转,黄苷(1 mM)可部分逆转。其他核苷不影响这种抑制作用。NSC 143019对DNA合成的抑制并非由于对RNA合成的抑制,反之亦然。NSC 143019抑制[8-14C]次黄嘌呤向酸溶性和酸不溶性鸟嘌呤核苷酸的转化,但不影响向腺嘌呤核苷酸的转化。从这些结果强烈表明,在NSC 143019浓度低于50μM时,该化合物的主要作用可能是在IMP转化为5'-磷酸黄苷这一步抑制GMP生物合成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验