Silva Cristina Duarte, Ramalhete Cátia, Spengler Gabriella, Mulhovo Silva, Molnar Joseph, Ferreira Maria-José U
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal.
Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003, Lisbon, Portugal; ATLÂNTICA - Instituto Universitário, Fábrica da Pólvora de Barcarena, 2730-036, Barcarena, Oeiras, Portugal.
Phytochemistry. 2022 Nov;203:113354. doi: 10.1016/j.phytochem.2022.113354. Epub 2022 Aug 6.
Aiming at overcoming multidrug resistance (MDR) in cancer, we have been studying Momordica balsamina, a vegetable known as African pumpkin. Five undescribed cucurbitane-type triterpenoids (balsaminaepoxide, balsaminatriol, balsaminoic acid, balsaminal, and balsaminol G) along with five known cucurbitacins were isolated from the methanol extract of Momordica balsamina aerial parts, whose structures were elucidated by spectroscopic data, mainly 1D and 2D NMR experiments. Compounds were evaluated for their ability as P-glycoprotein (P-gp/ABCB1) inhibitors in multidrug resistant human ABCB1-transfected mouse lymphoma cells (L5178Y, MDR) and resistant human colon adenocarcinoma cells (COLO 320), using the rhodamine-123 exclusion test, by flow cytometry. Several compounds, which were found to be non-cytotoxic, strongly inhibited P-gp efflux activity in a dose-dependent manner in both cell models. In MRD mouse lymphoma cells, balsaminol G and karavilagenin B were the most active, while in resistant colon adenocarcinoma cells, the strongest inhibitory activity was found for balsaminaepoxide, balsaminatriol and karavilagenin C, being several-fold more active than the positive control verapamil. In chemosensitivity assays, in a model of combination chemotherapy, selected compounds showed to interact synergistically with doxorubicin, thus substantiating their potential as MDR reversers. The strongest synergistic interaction was found for balsaminal and balsaminol G.
为了克服癌症中的多药耐药性(MDR),我们一直在研究苦瓜,一种被称为非洲南瓜的蔬菜。从苦瓜地上部分的甲醇提取物中分离出了五种未描述的葫芦素型三萜类化合物(苦瓜环氧醚、苦瓜三醇、苦瓜氨基酸、苦瓜醛和苦瓜醇G)以及五种已知的葫芦素,其结构通过光谱数据,主要是一维和二维核磁共振实验得以阐明。使用罗丹明 - 123排除试验,通过流式细胞术评估化合物在多药耐药的人ABCB1转染小鼠淋巴瘤细胞(L5178Y,MDR)和耐药人结肠腺癌细胞(COLO 320)中作为P - 糖蛋白(P - gp/ABCB1)抑制剂的能力。发现几种无细胞毒性的化合物在两种细胞模型中均以剂量依赖性方式强烈抑制P - gp外排活性。在MDR小鼠淋巴瘤细胞中,苦瓜醇G和卡拉维拉皂苷元B活性最强,而在耐药结肠腺癌细胞中,苦瓜环氧醚、苦瓜三醇和卡拉维拉皂苷元C的抑制活性最强,其活性比阳性对照维拉帕米高几倍。在联合化疗模型的化学敏感性测定中,选定的化合物显示出与阿霉素协同作用,从而证实了它们作为MDR逆转剂的潜力。苦瓜醛和苦瓜醇G的协同相互作用最强。