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灵芝三萜对 HeLa 细胞蛋白表达谱的影响。

Effects of triterpenes from Ganoderma lucidum on protein expression profile of HeLa cells.

机构信息

Shanghai Research Center for Modernization of Traditional Chinese Medicine, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, PR China.

出版信息

Phytomedicine. 2010 Jul;17(8-9):606-13. doi: 10.1016/j.phymed.2009.12.013. Epub 2010 Jan 25.

DOI:10.1016/j.phymed.2009.12.013
PMID:20092987
Abstract

To elucidate the cytotoxicity mechanism of Ganoderma triterpenes, a chemoproteomic study using five purified ganoderic acids, ganoderic acid F (GAF), ganoderic acid K (GAK), ganoderic B (GAB), ganoderic acid D (GAD) and ganoderic acid AM1 (GAAM1) was conducted. GAF, GAK, GAB, GAD and GAAM1 treatment for 48 h inhibited the proliferation of HeLa human cervical carcinoma cells with IC(50) values of 19.5+/-0.6 microM, 15.1+/-0.5 microM, 20.3+/-0.4 microM, 17.3+/-0.3 microM, 19.8+/-0.7 microM, respectively. The protein expression profiles of HeLa cells treated with each ganoderic acid at dose of 15 microM for 48 h were checked using two-dimensional electrophoresis (2-DE). The possible target-related proteins of ganoderic acids, i.e. proteins with same change tendency in all five ganoderic acids-treated groups compared with control, were identified using MALDI-TOF MS/MS. Twelve proteins including human interleukin-17E, eukaryotic translation initiation factor 5A (eIF5A), peroxiredoxin 2, ubiquilin 2, Cu/Zn-superoxide dismutase, 14-3-3 beta/alpha, TPM4-ALK fusion oncoprotein type 2, PP2A subunit A PR65-alpha isoform, nucleobindin-1, heterogeneous nuclear ribonucleoprotein K, reticulocalbin 1 and chain A of DJ-1 protein were identified. Ganoderic acids might exert their cytotoxicity by altering proteins involved in cell proliferation and/or cell death, carcinogenosis, oxidative stress, calcium signaling and ER stress.

摘要

为了阐明灵芝三萜的细胞毒性机制,采用化学蛋白质组学方法研究了 5 种纯化的灵芝酸,即灵芝酸 F(GAF)、灵芝酸 K(GAK)、灵芝酸 B(GAB)、灵芝酸 D(GAD)和灵芝酸 AM1(GAAM1)。GAF、GAK、GAB、GAD 和 GAAM1 处理 HeLa 人宫颈癌细胞 48 h,IC50 值分别为 19.5+/-0.6 μM、15.1+/-0.5 μM、20.3+/-0.4 μM、17.3+/-0.3 μM、19.8+/-0.7 μM。用 15 μM 各灵芝酸处理 HeLa 细胞 48 h,采用二维电泳(2-DE)检查细胞蛋白表达谱。采用 MALDI-TOF MS/MS 鉴定可能与灵芝酸相关的靶蛋白,即与对照相比在所有 5 种灵芝酸处理组中具有相同变化趋势的蛋白质。鉴定到 12 种蛋白,包括人白细胞介素-17E、真核翻译起始因子 5A(eIF5A)、过氧化物酶 2、泛素 2、Cu/Zn-超氧化物歧化酶、14-3-3β/α、TPM4-ALK 融合癌蛋白 2、PP2A 亚单位 A PR65-α同工型、核结合蛋白 1、异质核核糖核蛋白 K、网织钙蛋白 1 和 DJ-1 蛋白的 A 链。灵芝酸可能通过改变参与细胞增殖和/或细胞死亡、致癌作用、氧化应激、钙信号和 ER 应激的蛋白而发挥其细胞毒性作用。

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