Zhang Di, Wang Yinwen, Yu Peng, Sun Jiayi, Li Jingyang, Hu Yingfan, Meng Xianli, Li Juan, Xiang Li
State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Innovative Institute of Chinese Medicine and Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
The School of Preclinical Medicine, Chengdu University, Chengdu, 610106, China.
J Ethnopharmacol. 2025 Jan 30;337(Pt 2):118999. doi: 10.1016/j.jep.2024.118999. Epub 2024 Oct 28.
Scutellaria baicalensis Georgi, a widely used Chinese medicinal herb, has shown effectiveness against lung cancer. Scutellarein, a key component of Scutellaria baicalensis, also demonstrates anticancer properties in lung cancer. However, the underlying mechanisms have not yet been clarified.
This study aimed to investigate the effects of scutellarein in the treatment of NSCLC and its underlying mechanisms.
This study explored the effects of scutellarein on non-small cell lung cancer (NSCLC) and its mechanisms. A Lewis lung cancer mouse model was established to assess scutellarein's anticancer activity in vivo. Additionally, the compound's effects on cell proliferation, colony formation, migration, and apoptosis were evaluated in vitro using A549 and H1299 lung cancer cells. Metabolomics analysis was conducted to identify changes in cellular metabolism due to scutellarein, while molecular docking and western blotting techniques were employed to elucidate the molecular mechanisms of its anti-lung cancer effects.
Scutellarein significantly inhibited lung cancer xenograft tumor growth. In vitro studies showed that scutellarein suppressed migration and colony formation in A549 and H1299 cells, induced cell cycle arrest, and triggered cell apoptosis. Notably, scutellarein profoundly altered amino acid metabolism, particularly affecting glutamine metabolites. It affected key glutamine transporters ASCT2 and LAT1, as well as glutaminase GLS1, leading to their reduced expression.
Scutellarein effectively inhibits lung cancer growth both in vivo and in vitro by inducing cell apoptosis and downregulating the glutamine metabolic pathway.
黄芩是一种广泛使用的中药材,已显示出对肺癌的疗效。黄芩苷是黄芩的关键成分,在肺癌中也表现出抗癌特性。然而,其潜在机制尚未阐明。
本研究旨在探讨黄芩苷治疗非小细胞肺癌(NSCLC)的效果及其潜在机制。
本研究探讨了黄芩苷对非小细胞肺癌(NSCLC)的作用及其机制。建立Lewis肺癌小鼠模型以评估黄芩苷在体内的抗癌活性。此外,使用A549和H1299肺癌细胞在体外评估该化合物对细胞增殖、集落形成、迁移和凋亡的影响。进行代谢组学分析以确定黄芩苷引起的细胞代谢变化,同时采用分子对接和蛋白质印迹技术阐明其抗肺癌作用的分子机制。
黄芩苷显著抑制肺癌异种移植瘤的生长。体外研究表明,黄芩苷抑制A549和H1299细胞的迁移和集落形成,诱导细胞周期停滞,并引发细胞凋亡。值得注意的是,黄芩苷深刻改变了氨基酸代谢,尤其影响谷氨酰胺代谢产物。它影响关键的谷氨酰胺转运蛋白ASCT2和LAT1以及谷氨酰胺酶GLS1,导致它们的表达降低。
黄芩苷通过诱导细胞凋亡和下调谷氨酰胺代谢途径,在体内和体外均有效抑制肺癌生长。