Scutellarein inhibits lung cancer growth by inducing cell apoptosis and inhibiting glutamine metabolic pathway

IF 4.8 2区 医学 Q1 CHEMISTRY, MEDICINAL
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引用次数: 0

Abstract

Ethnopharmacological relevance

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.

Aim of the study

This study aimed to investigate the effects of scutellarein in the treatment of NSCLC and its underlying mechanisms.

Methods

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.

Results

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.

Conclusion

Scutellarein effectively inhibits lung cancer growth both in vivo and in vitro by inducing cell apoptosis and downregulating the glutamine metabolic pathway.

Abstract Image

黄芩苷通过诱导细胞凋亡和抑制谷氨酰胺代谢途径来抑制肺癌的生长。
民族药理学意义:黄芩是一种广泛使用的中药材,对肺癌有一定疗效。黄芩中的主要成分黄芩苷也具有抗肺癌的作用。然而,其潜在机制尚未明确:本研究旨在探讨黄芩苷治疗 NSCLC 的效果及其内在机制:本研究探讨了黄芩苷对非小细胞肺癌(NSCLC)的作用及其机制。通过建立路易斯肺癌小鼠模型来评估黄芩苷的体内抗癌活性。此外,还使用 A549 和 H1299 肺癌细胞在体外评估了该化合物对细胞增殖、集落形成、迁移和凋亡的影响。通过代谢组学分析确定了黄芩苷引起的细胞代谢变化,同时采用分子对接和 Western 印迹技术阐明了黄芩苷抗肺癌作用的分子机制:结果:黄芩苷能明显抑制肺癌异种移植瘤的生长。体外研究表明,黄芩苷能抑制 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,尤其影响了谷氨酰胺代谢产物。它影响了关键的谷氨酰胺转运体 ASCT2 和 LAT1 以及谷氨酰胺酶 GLS1,导致它们的表达减少:结论:通过诱导细胞凋亡和下调谷氨酰胺代谢途径,黄芩苷能有效抑制肺癌在体内和体外的生长。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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