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基于 HPLC 指纹图谱结合分子对接预测中药配方的抗肿瘤化学探针。

Prediction of anti-tumor chemical probes of a traditional Chinese medicine formula by HPLC fingerprinting combined with molecular docking.

机构信息

The Second People's Hospital of Fujian Province, Fuzhou, China.

Fujian University of Traditional Chinese Medicine, Fuzhou, China.

出版信息

Eur J Med Chem. 2014 Aug 18;83:294-306. doi: 10.1016/j.ejmech.2014.06.037. Epub 2014 Jun 18.

DOI:10.1016/j.ejmech.2014.06.037
PMID:24974349
Abstract

A traditional Chinese medicine formula (Fuzheng Yiliu decoction; FZYLD) has been used for many years in clinical settings to cure liver tumors; however, no empirical research has reported its chemical composition. In this paper, 21 chief constituents were distinguished from FZYLD using high-performance liquid chromatography-mass spectrometry fingerprint analysis. Molecular docking studies for B-cell lymphoma-extra large (Bcl-XL), interleukin (IL)-2, and tumor necrosis factor-α (TNF-α) were bound to evaluate their anticancer activities. 7 compounds showed potential Bcl-XL high affinity binding with a dissociate constant (Kd) < 10 μM; 7 compounds bound with IL-2 had a Kd < 10 μM; and 11 compounds showed potential TNF-α inhibition with a Kd < 10 μM. Moreover, 11 compounds showed better anticancer activity toward human HepG2 (hepatoma) cancer cell lines with IC50 values < 100 μM in vitro. The killings effects of natural killer cells can be activated by FZYLD on HepG2 cells and regulate the immune response through modulating IL-2 and TNF-α expression in vivo. In the "Fuzheng" Chinese medicine formula, many substances participate in the complex regulation of the immune network to execute the anti-tumor effect. The combination approach of chromatographic fingerprint and computer virtual docking used to explore active chemical matter of traditional Chinese medicine is extremely valuable.

摘要

一种中药方剂(扶正抑瘤汤;FZYLD)已在临床上用于治疗肝癌多年,但没有经验研究报道其化学成分。本文采用高效液相色谱-质谱指纹分析技术,从 FZYLD 中区分出 21 种主要成分。采用分子对接技术对 B 细胞淋巴瘤-特大(Bcl-XL)、白细胞介素(IL)-2 和肿瘤坏死因子-α(TNF-α)进行了结合研究,以评估其抗癌活性。7 种化合物与 Bcl-XL 具有高亲和力结合,解离常数(Kd)<10 μM;7 种化合物与 IL-2 结合,Kd<10 μM;11 种化合物对 TNF-α具有潜在的抑制作用,Kd<10 μM。此外,11 种化合物在体外对人 HepG2(肝癌)癌细胞系的抗癌活性更强,IC50 值<100 μM。FZYLD 可激活自然杀伤细胞对 HepG2 细胞的杀伤作用,并通过调节 IL-2 和 TNF-α的表达来调节免疫反应。在“扶正”中药方剂中,许多物质参与免疫网络的复杂调节,以发挥抗肿瘤作用。采用色谱指纹图谱和计算机虚拟对接相结合的方法来探索中药的活性物质具有很高的价值。

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