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新制癌菌素斯替马兰(YM881)的抗肿瘤机制。

Antitumor mechanisms of zinostatin stimalamer (YM881).

作者信息

Tanaka S, Yamamoto M, Numasaki Y

机构信息

Pharmacology Dept., Yamanouchi Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Res Commun Mol Pathol Pharmacol. 1996 May;92(2):165-76.

PMID:8774070
Abstract

The mechanism of antitumor action of zinostatin stimalamer (YM881) was studied. YM881 suppressed colony formation of HeLa cells dose-dependently, and showed cytocidal activity. The compound inhibited DNA synthesis, but neither RNA nor protein synthesis in L1210 cells, and induced cellular DNA strand breaks in HeLa cells and DNA cleavage of PM2 phage supercoiled DNA. The compound was also shown to cause typical G2/M phase arrest in the L1210 cell cycle, and inhibited activity of DNA polymerase alpha of HeLa cells, but only at a high concentration. These results suggest that the antitumor and cytotoxic mechanisms of YM881 are identical to those of neocarzinostatin (NCS), and were due to cellular DNA strand breaks induced by direct DNA-cleaving activity and the subsequent inhibition of DNA synthesis.

摘要

对新制癌菌素斯他莫霉素(YM881)的抗肿瘤作用机制进行了研究。YM881剂量依赖性地抑制HeLa细胞的集落形成,并表现出杀细胞活性。该化合物抑制L1210细胞中的DNA合成,但不抑制RNA和蛋白质合成,且诱导HeLa细胞中的细胞DNA链断裂以及PM2噬菌体超螺旋DNA的DNA裂解。该化合物还显示出在L1210细胞周期中引起典型的G2/M期阻滞,并抑制HeLa细胞的DNA聚合酶α活性,但仅在高浓度时才会抑制。这些结果表明,YM881的抗肿瘤和细胞毒性机制与新制癌菌素(NCS)相同,是由于直接DNA裂解活性诱导的细胞DNA链断裂以及随后对DNA合成的抑制所致。

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