Li Yurong, Wei Juanjuan, Ye Zimao, Ji Chen, Li Wenji, Xu Li, Zhou Zhiqin
Key Laboratory of Agricultural Biosafety and Green Production of Upper Yangtze River (Ministry of Education), College of Horticulture and Landscape Architecture, Southwest University, Beibei District, Chongqing 400715, China.
School of Design, Chongqing Industry Polytechnic College, Chongqing 401120, China.
Antioxidants (Basel). 2024 Dec 25;14(1):11. doi: 10.3390/antiox14010011.
Citrus peel essential oils (CPEOs) have demonstrated substantial medicinal potential for glioblastoma treatment because of their extensive antitumor effects, low potential for drug resistance, and ability to cross the human blood-brain barrier. In this study, the chemical compositions of five CPEOs were analyzed via gas chromatography-mass spectrometry (GC-MS). CCK8 assays were used to evaluate the ability of five CPEOs to inhibit U251 human glioblastoma cells, and XLB and RA were selected for further investigation. Through wound healing assays and cell cycle and apoptosis analyses via flow cytometry, it was revealed that these CPEOs inhibited cell migration, arrested the cell cycle at G1/G0, and induced apoptosis with similar levels of inhibition. After CPEOs treatment, the intracellular Ca content and reactive oxygen species levels in U251 cells increased significantly, whereas the mitochondrial membrane potential decreased. Additionally, the antioxidant enzyme system (SOD, POD, CAT, and GR) and the nonenzymatic defense system (GSH) were inhibited, leading to an increase in lipid peroxidation. qRT-PCR indicated the significant upregulation of intracellular calcium ion signaling pathways and the upregulation of mitochondrial apoptosis-related genes. Additionally, the activation of calcicoptosis-related indicators induced by the CPEOs could be reversed by inhibitor treatment, confirming that both of the selected CPEOs inhibit tumors by activating calcicoptosis-related pathways. These findings highlight the immense potential of CPEOs in healthcare and pharmaceutical applications by not only providing a scientific basis for the potential application of CPEOs in the treatment of glioblastoma but also offering new insights for the development of novel antitumor drugs.
柑橘皮精油(CPEOs)因其广泛的抗肿瘤作用、低耐药性以及能够穿越人体血脑屏障,已显示出在胶质母细胞瘤治疗方面具有巨大的药用潜力。在本研究中,通过气相色谱 - 质谱联用(GC - MS)分析了五种CPEOs的化学成分。采用CCK8法评估五种CPEOs抑制U251人胶质母细胞瘤细胞的能力,并选择XLB和RA作进一步研究。通过伤口愈合试验以及流式细胞术进行细胞周期和凋亡分析,结果显示这些CPEOs抑制细胞迁移,使细胞周期停滞在G1/G0期,并诱导凋亡,且抑制水平相似。CPEOs处理后,U251细胞内的钙含量和活性氧水平显著升高,而线粒体膜电位降低。此外,抗氧化酶系统(超氧化物歧化酶、过氧化物酶、过氧化氢酶和谷胱甘肽还原酶)和非酶防御系统(谷胱甘肽)受到抑制,导致脂质过氧化增加。qRT - PCR表明细胞内钙离子信号通路显著上调以及线粒体凋亡相关基因上调。此外,抑制剂处理可逆转CPEOs诱导的钙凋亡相关指标的激活,证实所选的两种CPEOs均通过激活钙凋亡相关途径抑制肿瘤。这些发现突出了CPEOs在医疗保健和制药应用中的巨大潜力,不仅为CPEOs在胶质母细胞瘤治疗中的潜在应用提供了科学依据,也为新型抗肿瘤药物的开发提供了新的见解。