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Genotoxicity of streptozotocin.

机译:链脲佐菌素的遗传毒性。

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摘要

Streptozotocin (Streptozocin, STZ, CAS No. 18883-66-4) is a monofunctional nitrosourea derivative isolated from Streptomyces achromogenes. It has broad spectrum antibiotic activity and antineoplastic properties and is often used to induce diabetes mellitus in experimental animals through its toxic effects on pancreatic beta cells. STZ is a potent alkylating agent known to directly methylate DNA and is highly genotoxic, producing DNA strand breaks, alkali-labile sites, unscheduled DNA synthesis, DNA adducts, chromosomal aberrations, micronuclei, sister chromatid exchanges, and cell death. This antibiotic was found to be mutagenic in bacterial assays and eukaryotic cells. STZ is also carcinogenic; a single administration induces tumors in rat kidney, liver, and pancreas. Several lines of evidence indicate that free radicals are involved in the production of DNA and chromosome damage by this compound. Because of the use of STZ as an antineoplastic agent, the study of its genotoxicity has considerable practical significance. The purpose of this review is to present our current knowledge regarding the genotoxicity of STZ.
机译:链脲佐菌素(Streptozocin,STZ,CAS No.18883-66-4)是从产色链霉菌分离的单官能亚硝基脲衍生物。它具有广谱抗生素活性和抗肿瘤特性,并且由于其对胰腺β细胞的毒性作用,常被用于在实验动物中诱导糖尿病。 STZ是一种有效的烷基化剂,已知可以直接将DNA甲基化,并且具有很高的遗传毒性,可产生DNA链断裂,碱不稳定位点,计划外的DNA合成,DNA加合物,染色体畸变,微核,姐妹染色单体交换和细胞死亡。在细菌检测和真核细胞中发现这种抗生素具有致突变性。 STZ也是致癌的。一次给药可在大鼠肾脏,肝脏和胰腺中诱发肿瘤。几条证据表明,自由基参与了该化合物的DNA产生和染色体损伤。由于将STZ用作抗肿瘤药,对其遗传毒性的研究具有相当大的现实意义。这篇综述的目的是介绍我们目前有关STZ遗传毒性的知识。

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