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倍半萜多杀菌素的合成与生物学研究:9-表多杀菌素对耐药癌细胞的活性

Synthetic and Biological Studies of Sesquiterpene Polygodial: Activity of 9-Epipolygodial against Drug-Resistant Cancer Cells.

作者信息

Dasari Ramesh, De Carvalho Annelise, Medellin Derek C, Middleton Kelsey N, Hague Frédéric, Volmar Marie N M, Frolova Liliya V, Rossato Mateus F, De La Chapa Jorge J, Dybdal-Hargreaves Nicholas F, Pillai Akshita, Mathieu Véronique, Rogelj Snezna, Gonzales Cara B, Calixto João B, Evidente Antonio, Gautier Mathieu, Munirathinam Gnanasekar, Glass Rainer, Burth Patricia, Pelly Stephen C, van Otterlo Willem A L, Kiss Robert, Kornienko Alexander

机构信息

Department of Chemistry and Biochemistry, Texas State University, San Marcos, TX, 78666, USA.

Laboratoire de Cancérologie et de Toxicologie Expérimentale, Faculté de Pharmacie, Université Libre de Bruxelles, 1050, Brussels, Belgium.

出版信息

ChemMedChem. 2015 Dec;10(12):2014-26. doi: 10.1002/cmdc.201500360. Epub 2015 Oct 5.

Abstract

Polygodial, a terpenoid dialdehyde isolated from Polygonum hydropiper L., is a known agonist of the transient receptor potential vanilloid 1 (TRPV1). In this investigation a series of polygodial analogues were prepared and investigated for TRPV1-agonist and anticancer activities. These experiments led to the identification of 9-epipolygodial, which has antiproliferative potency significantly exceeding that of polygodial. 9-Epipolygodial was found to maintain potency against apoptosis-resistant cancer cells as well as those displaying the multidrug-resistant (MDR) phenotype. In addition, the chemical feasibility for the previously proposed mechanism of action of polygodial, involving the formation of a Paal-Knorr pyrrole with a lysine residue on the target protein, was demonstrated by the synthesis of a stable polygodial pyrrole derivative. These studies reveal rich chemical and biological properties associated with polygodial and its direct derivatives. These compounds should inspire further work in this area aimed at the development of new pharmacological agents, or the exploration of novel mechanisms of covalent modification of biological molecules with natural products.

摘要

水蓼二醛是一种从水蓼中分离得到的萜类二醛,是已知的瞬时受体电位香草酸亚型1(TRPV1)激动剂。在本研究中,制备了一系列水蓼二醛类似物,并对其TRPV1激动剂活性和抗癌活性进行了研究。这些实验鉴定出了9-表水蓼二醛,其抗增殖能力显著超过水蓼二醛。研究发现,9-表水蓼二醛对凋亡抗性癌细胞以及表现出多药耐药(MDR)表型的癌细胞均具有活性。此外,通过合成一种稳定的水蓼二醛吡咯衍生物,证明了先前提出的水蓼二醛作用机制(涉及与靶蛋白上的赖氨酸残基形成Paal-Knorr吡咯)在化学上的可行性。这些研究揭示了与水蓼二醛及其直接衍生物相关的丰富化学和生物学特性。这些化合物应能激发该领域进一步的研究工作,旨在开发新的药物,或探索天然产物对生物分子进行共价修饰的新机制。

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