Grupo de Investigaciones Biomédicas y de Genética Humana Aplicada (GIBGA), Laboratorio de Biología Celular y Molecular, Facultad de Ciencias de la Salud, Universidad de Ciencias Aplicadas y Ambientales (U.D.C.A), Calle 222 # 55-37, Bogotá 111166, Colombia.
Grupo de Investigación en Ciencias Exactas, Física y Naturales Aplicadas, Facultad de Ciencias Básicas y Biomédicas, Laboratorio de Simulación Molecular y Bioinformática, Universidad Simón Bolívar, Carrera 59 # 59-65, Barranquilla 080002, Colombia.
Int J Mol Sci. 2023 Oct 14;24(20):15185. doi: 10.3390/ijms242015185.
() R. M. King and H. Rob () contains bioactive flavonoids that may have antioxidant and/or anti-cancer properties. This study investigated the potential anti-cancer properties of a newly identified chalcone isolated from the inflorescences of the plant () R. M. King and H. Rob (). The chalcone structure was determined using HPLC/MS (QTOF), UV, and NMR spectroscopy. The compound cytotoxicity and selectivity were evaluated on prostate, cervical, and breast cancer cell lines using the MTT assay. Apoptosis and autophagy induction were assessed through flow cytometry by detecting annexin V/7-AAD, active Casp3/7, and LC3B proteins. These results were supported by Western blot analysis. Mitochondrial effects on membrane potential, as well as levels of pro- and anti-apoptotic proteins were analyzed using flow cytometry, fluorescent microscopy, and Western blot analysis specifically on a triple-negative breast cancer (TNBC) cell line. Furthermore, molecular docking (MD) and molecular dynamics (MD) simulations were performed to evaluate the interaction between the compounds and pro-survival proteins. The compound identified as 2',3,4-trihydroxy-4',6'-dimethoxy chalcone inhibited the cancer cell line proliferation and induced apoptosis and autophagy. MDA-MB-231, a TNBC cell line, exhibited the highest sensitivity to the compound with good selectivity. This activity was associated with the regulation of mitochondrial membrane potential, activation of the pro-apoptotic proteins, and reduction of anti-apoptotic proteins, thereby triggering the intrinsic apoptotic pathway. The chalcone consistently interacted with anti-apoptotic proteins, particularly the Bcl-2 protein, throughout the simulation period. However, there was a noticeable conformational shift observed with the negative autophagy regulator mTOR protein. Future studies should focus on the molecular mechanisms underlying the anti-cancer potential of the new chalcone and other flavonoids from , particularly against predominant cancer cell types.
从植物 () R. M. King 和 H. Rob() 的花序中分离出一种新的查尔酮,本研究探讨了其潜在的抗癌特性。查尔酮结构通过 HPLC/MS(QTOF)、UV 和 NMR 光谱确定。采用 MTT 法测定该化合物对前列腺癌、宫颈癌和乳腺癌细胞系的细胞毒性和选择性。通过流式细胞术检测 annexin V/7-AAD、活性 Casp3/7 和 LC3B 蛋白评估细胞凋亡和自噬的诱导。Western blot 分析支持这些结果。通过流式细胞术、荧光显微镜和 Western blot 分析专门针对三阴性乳腺癌(TNBC)细胞系,分析线粒体对膜电位的影响以及促凋亡和抗凋亡蛋白的水平。此外,还进行了分子对接(MD)和分子动力学(MD)模拟,以评估化合物与促生存蛋白之间的相互作用。鉴定出的化合物 2',3,4-三羟基-4',6'-二甲氧基查尔酮抑制癌细胞系增殖并诱导细胞凋亡和自噬。MDA-MB-231,一种 TNBC 细胞系,对该化合物表现出最高的敏感性和良好的选择性。这种活性与调节线粒体膜电位、激活促凋亡蛋白和减少抗凋亡蛋白有关,从而触发内在凋亡途径。查尔酮在整个模拟过程中与抗凋亡蛋白(尤其是 Bcl-2 蛋白)持续相互作用。然而,与负自噬调节剂 mTOR 蛋白观察到明显的构象变化。未来的研究应侧重于新查尔酮和 的其他类黄酮的抗癌潜力的分子机制,特别是针对主要的癌细胞类型。