化学成分分析、通过诱导 MCF-7 细胞凋亡的细胞毒性活性及树皮非极性提取物的分子对接。
Chemical profiling, cytotoxic activities through apoptosis induction in MCF-7 cells and molecular docking of bark nonpolar extract.
机构信息
Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt.
Garden for Medicinal Plants, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
出版信息
J Biomol Struct Dyn. 2022;40(20):9636-9647. doi: 10.1080/07391102.2021.1932599. Epub 2021 Jun 2.
The chemical constituents of the nonpolar fractions of the bamboo shoot skin were extensively studied. The phytochemical study was divided into two parts: the first deals with isolation of the chemical constituents using different chromatographic techniques that resulted in isolation of four compounds. The chemical structures of the pure isolated compounds were elucidated using different spectroscopic data. The second part deals with identification of the rest of the constituents using the GC technique. Additionally, both crude extract and the pure isolated compounds were investigated for cytotoxic activity. One of the isolated compounds; namely glyceryl 1-monopalmitate showed highly promising effect against the MCF-7 cells with (IC = 19.78 µM) compared to 5-FU (26.98 µM), and it remarkably stimulated apoptotic breast cancer cell death with 31.6-fold (16.13% compared to 0.51 for the control) at pre-G1 and G2/M-phase cell cycle arrest and blocked the progression of MCF-7 cells. Moreover, the identified compounds especially were found to have high binding affinity towards both TPK and VEGFR-2 through the molecular docking studies which highlight its mode of action. HighlightsChemical profiling of bark nonpolar extract was fully identified.Glyceryl 1-monopalmitate showed highly promising effect against the MCF-7 cells with (IC = 19.78 µM) compared to 5-FU (26.98 µM).Glyceryl 1-monopalmitate significantly stimulated apoptotic breast cancer cell death with 31.6-fold by arresting cell cycle at G2/M and preG1 phases.Molecular docking simulation showed good binding affinities towards TPK and VEGFR-2 proteins.Communicated by Ramaswamy H. Sarma.
竹笋皮非极性部位的化学成分进行了广泛的研究。植物化学研究分为两部分:第一部分涉及使用不同的色谱技术分离化学成分,这导致分离出四种化合物。通过不同的光谱数据阐明了纯分离化合物的化学结构。第二部分涉及使用 GC 技术鉴定其余成分。此外,还研究了粗提取物和纯分离化合物的细胞毒性活性。分离出的化合物之一;即甘油 1-单棕榈酸酯对 MCF-7 细胞具有很高的抗肿瘤活性(IC = 19.78 μM),与 5-FU(26.98 μM)相比,它显著刺激乳腺癌细胞凋亡,凋亡率为 31.6 倍(与对照相比为 0.51),在 G1 期和 G2/M 期细胞周期阻滞前,阻止 MCF-7 细胞的进展。此外,通过分子对接研究发现,鉴定出的化合物特别是对 TPK 和 VEGFR-2 具有高结合亲和力,这突出了其作用模式。亮点对树皮非极性提取物进行了全面的化学成分分析。与 5-FU(26.98 μM)相比,甘油 1-单棕榈酸酯对 MCF-7 细胞具有很高的抗肿瘤活性(IC = 19.78 μM)。甘油 1-单棕榈酸酯通过在 G2/M 和 G1 期阻滞细胞周期,显著刺激 31.6 倍的乳腺癌细胞凋亡。分子对接模拟显示对 TPK 和 VEGFR-2 蛋白具有良好的结合亲和力。由 Ramaswamy H. Sarma 传达。