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棘皮菌素,一种海洋天然化合物,可抑制多种癌细胞系的细胞运动。

Sceptrin, a marine natural compound, inhibits cell motility in a variety of cancer cell lines.

机构信息

Cancer Center, Burnham Institute for Medical Research, 10901 North Torrey Pines Rd., La Jolla, California, USA.

出版信息

ACS Chem Biol. 2010 Feb 19;5(2):195-202. doi: 10.1021/cb900240k.

Abstract

Sceptrin, a natural compound produced by various marine sponges, was tested for its effect on cell motility. We report for the first time that sceptrin inhibits cell motility in several cancer cell lines. The compound shows no toxicity at concentrations that are double the amount of sceptrin required for maximal inhibitory effect. Both random and factor-induced migration were impaired, suggesting that sceptrin targets a central process of cell motility machinery. Activity of de novo synthesized sceptrin was indistinguishable from sceptrin purified from Agelas nakamurai, and the inhibitory activity was found to be, at least partially, due to sceptrin's capability to inhibit cell contractility. Additionally, sceptrin was found to bind to monomeric actin, further suggesting a mechanism involving the actin cytoskeleton. Close analogues of sceptrin were synthesized, tested for their effect on cell motility, and found to be either equimolar or less potent compared to the parental compound. Inadvertent cell motility is a key contributing factor in various human diseases, including cancer and chronic inflammation. Marine compounds isolated from sponges have been proven to be an excellent source of metabolites that show biological activities. Given the recently achieved total synthesis of sceptrin in multigram quantities, sceptrin could prove to be an attractive lead molecule for further preclinical testing and development for therapeutic purposes, as well as a useful research tool to elucidate the mechanisms involved in cell motility.

摘要

海绵天然产物 sceptrin 抑制多种癌细胞的迁移运动

海绵天然产物 sceptrin 抑制多种癌细胞的迁移运动

海绵天然产物 sceptrin 可抑制多种癌细胞的迁移运动

我们首次报道 sceptrin 可抑制多种癌细胞的迁移运动。该化合物在产生最大抑制效果所需 sceptrin 浓度两倍的浓度下无细胞毒性。随机迁移和诱导迁移均受到抑制,提示 sceptrin 靶向细胞迁移机制的核心过程。从头合成的 sceptrin 与从 Agelas nakamurai 中纯化的 sceptrin 活性相同,抑制活性至少部分归因于 sceptrin 抑制细胞收缩的能力。此外,还发现 sceptrin 可与单体肌动蛋白结合,这进一步提示了一种涉及肌动蛋白细胞骨架的机制。合成了 sceptrin 的类似物,并测试了它们对细胞迁移的影响,发现它们与母体化合物的摩尔效价相等或更低。在各种人类疾病中,包括癌症和慢性炎症,细胞迁移的失控是一个关键的致病因素。从海绵中分离出的海洋化合物已被证明是具有生物活性的代谢物的极好来源。鉴于 sceptrin 最近已实现了克级规模的全合成,sceptrin 可能成为进一步进行临床前测试和开发治疗用途的有吸引力的先导分子,同时也是阐明细胞迁移机制的有用研究工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9992/2825093/a3865d646841/cb-2009-00240k_0005.jpg

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