Department of Pharmaceutical Biology, Institute of Pharmacy and Biochemistry, University of Mainz, 55128 Mainz, Germany.
BMC Complement Altern Med. 2014 Sep 19;14:340. doi: 10.1186/1472-6882-14-340.
The search for natural products as potential cytotoxic agents has yielded promising candidates. However multidrug resistance (MDR) is still a major hurdle for patients receiving chemotherapy. In the present study, we evaluated the cytotoxicity of the methanol extracts of four dietary Aframomum plant species (A. arundinaceum, A. alboviolaceum, A. kayserianum and A. polyanthum) against nine sensitive and MDR cancer cell lines. We have also identified the bioactive constituents of A. arundinaceum.
The cytotoxicity of the methanol extracts of the above plants was determined using a resazurin reduction assay. Chromatographic techniques were used to isolate the constituents of A. arundinaceum.
A preliminary experiment on leukemia CCRF-CEM cells at 40 μg/mL showed that the extracts from A. kayserianum and A. alboviolaceum as well as the isolated compounds namely compounds aframodial (1), 8(17),12-labdadien-15,16-dial (2), galanolactone (3), 1-p-menthene-3,6-diol (6) and 1,4-dimethoxybenzene (7) were less active, inducing more than 50% growth of this cell line contrary to A. polyanthum and A. arundinaceum extracts, galanals A (4) and B (5), naringenin (8) and kaempferol-3,7,4'-trimethylether (9). The IC50 values below or around 30 μg/mL were recorded with A. arundinaceum extract against eight of the nine tested cancer cell lines. This extract as well as compound 8 displayed IC50 values below 40 μg/mL towards the nine tested cancer cell lines whilst A. polyanthum extract, compounds 4, 5 and 9 showed selective activities. Collateral sensitivity (hypersensitivity) was observed with A. arundinaceum extract towards leukemia CEM/ADR5000 cells and glioblastoma U87MG.ΔEGFR compared to their respective sensitive counterparts CEM/CEM and U87MG.
The results of this study provide evidence of the cytotoxicity selected Aframomum species as well as a baseline information for the potential use of Aframomum arundinaceum in the fight against drug sensitive and otherwise drug-resistant cancers.
寻找天然产物作为潜在的细胞毒性剂已经产生了有前途的候选物。然而,多药耐药(MDR)仍然是接受化疗的患者的主要障碍。在本研究中,我们评估了四种食用 Aframomum 植物(A. arundinaceum、A. alboviolaceum、A. kayserianum 和 A. polyanthum)甲醇提取物对九种敏感和 MDR 癌细胞系的细胞毒性。我们还鉴定了 A. arundinaceum 的生物活性成分。
使用 Resazurin 还原测定法测定上述植物甲醇提取物的细胞毒性。采用色谱技术分离 A. arundinaceum 的成分。
在 40μg/mL 的白血病 CCRF-CEM 细胞的初步实验中,结果表明,Kayserianum 和 Alboviolaceum 种的提取物以及分离的化合物 namely aframodial(1)、8(17)、12-labdadien-15、16-dial(2)、galanolactone(3)、1-p-menthene-3,6-diol(6)和 1,4-dimethoxybenzene(7)活性较低,导致该细胞系的生长超过 50%,而 A. polyanthum 和 A. arundinaceum 提取物、galanals A(4)和 B(5)、naringenin(8)和 kaempferol-3,7,4'-trimethylether(9)则不然。在 9 种测试的癌细胞系中,A. arundinaceum 提取物的 IC50 值低于或约为 30μg/mL。该提取物和化合物 8 对 9 种测试的癌细胞系的 IC50 值低于 40μg/mL,而 A. polyanthum 提取物、化合物 4、5 和 9 则表现出选择性活性。与各自敏感对照物 CEM/CEM 和 U87MG 相比,A. arundinaceum 提取物对白血病 CEM/ADR5000 细胞和神经胶质瘤 U87MG.ΔEGFR 表现出交叉敏感性(超敏性)。
本研究结果提供了选定 Aframomum 物种的细胞毒性证据,并为 Aframomum arundinaceum 在对抗敏感和耐药性癌症方面的潜在用途提供了基线信息。