Student Research Committee, Kerman University of Medical Science, Kerman, Iran.
Herbal and Traditional Medicines Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Appl Biochem Biotechnol. 2023 May;195(5):3327-3344. doi: 10.1007/s12010-022-04301-z. Epub 2022 Dec 31.
Over recent years, much attention has been devoted to the field of screening natural products and/or their novel structures because of reversing cancer progression. The current research work was intended to explore the cytotoxic activity of ethanol and ethyl acetate extracts of dried fruit of Terminalia chebula Retz. (T. chebula) in MCF-7 cell line. High-performance thin-layer chromatographic (HPTLC) method and Folin-Ciocalteu colorimetric techniques were performed. Anti-proliferative activities of T. chebula fruit extracts on the MCF-7 cell line were evaluated using MTT assay. Effects of both extracts on the migration of MCF-7 cells and the size of MCF-7-derived spheroids were also evaluated. Moreover, antioxidant properties were measured by DPPH and FRAP methods. Western blotting was used to measure the HIF-1α and CXCR-4 protein levels. Chebulagic acid, gallic acid, chebulinic acid, and ellagic acid were found as major compounds in both extracts. The total phenolic contents based on gallic acid equivalent (GAE) in the ethanol and ethyl acetate extracts of T. chebula were found to be 453.68 ± 0.31 and 495.12 ± 0.43 mg GAE/g dry weight of the extract, respectively. Both extracts exerted a significant dose- and time-dependent cytotoxicity effect on MCF-7 cells. They also had a marked negative effect on the average size of MCF-7-derived spheroids and their migration rate. None of the extracts exhibited stronger antioxidant activities than vitamin C. Furthermore, both extracts at a concentration of 125 µg/ml could meaningfully decrease the expression levels of HIF-1α and CXCR-4 in MCF-7 cells. These data represent that T. chebula may be a valuable medicinal resource in the regulation of breast cancer proliferation, growth, and metastasis.
近年来,人们非常关注从天然产物中筛选具有新颖结构的化合物,以逆转癌症的进展。本研究旨在探索诃子干果的乙醇和乙酸乙酯提取物在 MCF-7 细胞系中的细胞毒性活性。采用高效薄层色谱(HPTLC)法和福林-酚比色法进行研究。采用 MTT 法评估 T. chebula 果实提取物对 MCF-7 细胞系的抗增殖活性。还评估了两种提取物对 MCF-7 细胞迁移和 MCF-7 衍生球体大小的影响。此外,还通过 DPPH 和 FRAP 法测量抗氧化性能。使用 Western blotting 测量 HIF-1α 和 CXCR-4 蛋白水平。在两种提取物中均发现诃子酸、没食子酸、诃子酸和鞣花酸为主要化合物。基于没食子酸当量(GAE)的乙醇和乙酸乙酯提取物中 T. chebula 的总酚含量分别为 453.68±0.31 和 495.12±0.43 mg GAE/g 提取物干重。两种提取物对 MCF-7 细胞均表现出显著的剂量和时间依赖性细胞毒性作用。它们还对 MCF-7 衍生球体的平均大小及其迁移率产生显著的负影响。两种提取物的抗氧化活性均弱于维生素 C。此外,两种提取物在 125 µg/ml 的浓度下可显著降低 MCF-7 细胞中 HIF-1α 和 CXCR-4 的表达水平。这些数据表明,诃子可能是调节乳腺癌增殖、生长和转移的有价值的药用资源。