Kohno Toshitaka, Hai-Bang Tran, Zhu Qinchang, Amen Yhiya, Sakamoto Seiichi, Tanaka Hiroyuki, Morimoto Satoshi, Shimizu Kuniyoshi
Division of Systematic Forest and Forest Products Sciences, Department of Agro-Environmental Sciences, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka, 812-8581, Japan.
Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, 812-8582, Japan.
J Nat Med. 2017 Apr;71(2):457-462. doi: 10.1007/s11418-017-1072-y. Epub 2017 Jan 11.
Tubulin polymerization is an important target for anticancer therapies. Even though the potential of Ganoderma triterpenoids against various cancer targets had been well documented, studies on their tubulin polymerization-stimulating activity are scarce. This study was conducted to evaluate the effect of Ganoderma triterpenoids on tubulin polymerization. A total of twenty-four compounds were investigated using an in vitro tubulin polymerization assay. Results showed that most of the studied triterpenoids exhibited microtuble-stabilizing activity to different degrees. Among the investigated compounds, ganoderic acid T-Q, ganoderiol F, ganoderic acid S, ganodermanontriol and ganoderic acid TR were found to have the highest activities. A structure-activity relationship (SAR) analysis was performed. Extensive investigation of the SAR suggests the favorable structural features for the tubulin polymerization-stimulating activity of lanostane triterpenes. These findings would be helpful for further studies on the potential mechanisms of the anticancer activity of Ganoderma triterpenoids and give some indications on the design of tubulin-targeting anticancer agents.
微管蛋白聚合是抗癌治疗的一个重要靶点。尽管灵芝三萜对各种癌症靶点的潜在作用已有充分记载,但关于其刺激微管蛋白聚合活性的研究却很少。本研究旨在评估灵芝三萜对微管蛋白聚合的影响。使用体外微管蛋白聚合试验对总共24种化合物进行了研究。结果表明,大多数研究的三萜类化合物都表现出不同程度的微管稳定活性。在所研究的化合物中,发现灵芝酸T-Q、灵芝二醇F、灵芝酸S、灵芝三醇和灵芝酸TR具有最高活性。进行了构效关系(SAR)分析。对构效关系的广泛研究表明了羊毛甾烷型三萜刺激微管蛋白聚合活性的有利结构特征。这些发现将有助于进一步研究灵芝三萜抗癌活性的潜在机制,并为靶向微管蛋白的抗癌药物设计提供一些指导。