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新型氨肽酶 N(APN/CD13)抑制剂 24F 可抑制肝癌细胞的侵袭和血管生成。

Novel aminopeptidase N (APN/CD13) inhibitor 24F can suppress invasion of hepatocellular carcinoma cells as well as angiogenesis.

机构信息

Hepato-Biliary-Pancreatic Surgery Division, Department of Surgery, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.

出版信息

Biosci Trends. 2010 Apr;4(2):56-60.

Abstract

Aminopeptidase N (APN)/CD13 is a widely expressed transmembrane protein and its altered expression has been detected in various cancer cells. Several APN inhibitors have been developed and some of them have been found to have effectiveness as anti-cancer agents. This article reports anti-cancer effects of a hydroxamic acid derivative 24F that was newly-synthesized as an APN inhibitor. 24F had the ability to inhibit the invasion of hepatocellular carcinoma (HCC) cell line HuH-7, although the growth of HuH-7 was not significantly inhibited at the analyzed concentrations of 24F and incubation times used. Furthermore, incubation of vascular endothelial cells with 24F was found to be effective for the suppression of the angiogenic phenomenon. These results suggest that the novel APN inhibitor 24F may work as an anti-cancer agent for HCC via inhibition of HCC cell invasion and angiogenesis.

摘要

氨基肽酶 N(APN)/CD13 是一种广泛表达的跨膜蛋白,其在各种癌细胞中的表达发生了改变。已经开发了几种 APN 抑制剂,其中一些已被发现具有作为抗癌剂的有效性。本文报道了新合成的 APN 抑制剂羟肟酸衍生物 24F 的抗癌作用。24F 具有抑制肝癌(HCC)细胞系 HuH-7 侵袭的能力,尽管在分析的 24F 浓度和孵育时间下,HuH-7 的生长没有明显受到抑制。此外,发现血管内皮细胞与 24F 孵育可有效抑制血管生成现象。这些结果表明,新型 APN 抑制剂 24F 可能通过抑制 HCC 细胞侵袭和血管生成而作为 HCC 的抗癌剂发挥作用。

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