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首页> 外文期刊>International journal of molecular medicine >Antitumor activity of asukamycin, a secondary metabolite from the actinomycete bacterium Streptomyces nodosus subspecies asukaensis.
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Antitumor activity of asukamycin, a secondary metabolite from the actinomycete bacterium Streptomyces nodosus subspecies asukaensis.

机译:Asukamycin的抗肿瘤活性,Asukamycin是放线菌细菌Noeptsus nodosus亚种asukaensis的次生代谢产物。

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摘要

Asukamycin, a manumycin-type metabolite, was isolated by a rapid and easily scalable purification scheme. Thus far, studies on the biological activity of asukamycin have been limited to its role as an antibacterial and antifungal agent. By using five different tumor cell lines we demonstrate antineoplastic activity of asukamycin. It inhibited cell growth at concentrations similar to other members of the manumycin family (IC50 1-5 microM). Cytotoxicity of asukamycin was accompanied by activation of caspases 8 and 3 and was diminished by SB 202190, a specific p38 mitogen-activated protein kinase (MAPK) inhibitor. These data, in combination with earlier observations showing its low in vivo toxicity, indicate that further studies on the potential antitumor activity of asukamycin are warranted.
机译:通过快速且易于扩展的纯化方案分离出了菊粉型代谢产物明日香霉素。迄今为止,关于明日香霉素的生物活性的研究仅限于其作为抗菌和抗真菌剂的作用。通过使用五种不同的肿瘤细胞系,我们证明了明日霉素的抗肿瘤活性。它以与Manumycin家族其他成员相似的浓度(IC50 1-5 microM)抑制细胞生长。 Asukamycin的细胞毒性伴随半胱天冬酶8和3的活化而被SB 202190(一种特定的p38丝裂原活化蛋白激酶(MAPK)抑制剂)减弱。这些数据,结合显示低体内毒性的早期观察结果,表明有必要进一步研究明日霉素的潜在抗肿瘤活性。

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