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羽扇豆醇通过抑制肺癌中 MAPK/ERK 通路发挥抗转移作用。

Anti-Metastatic Effects of Lupeol via the Inhibition of MAPK/ERK Pathway in Lung Cancer.

机构信息

Bapalal Vaidya Botanical Research Centre, Department of Biosciences, Veer Narmad South Gujarat University, Surat, Gujarat, India.

Department of Biology, College of Science, University of Ha'il, Ha'il, P O Box 2440, Saudi Arabia.

出版信息

Anticancer Agents Med Chem. 2021;21(2):201-206. doi: 10.2174/1871520620666200424131548.

Abstract

BACKGROUND AND OBJECTIVE

ERK pathway is one of the most crucial pathways in lung cancer metastasis. Targeting its pathway is decisive in lung cancer research. Thus, this study demonstrated for the first time for significant and selective anti-metastatic effects of lupeol against lung cancer A549 cells via perturbations in the ERK signaling pathway.

MATERIALS AND METHODS

Human protein targets of lupeol were predicted in silico. Migration and cytotoxicity assays were carried out in vitro. Expression levels of proteins Erk1/2 and pErk1/2 were ensured using Enzyme- Linked Immunosorbent Assay (ELISA). Semi-quantitative RT-PCR technique was used to estimate changes in crucial mesenchymal marker gene expression levels of N-cadherin and vimentin.

RESULTS

Lupeol was found to target ERK and MEK proteins effectively. Despite having no cytotoxic effects, lupeol also significantly inhibited cell migration in A549 cells with decreased expression of the pErk1/2 protein along with N-cadherin and vimentin genes.

CONCLUSION

Lupeol inhibits cell migration, showed no cytotoxic effects on A549 cells, decreased pErk1/2 and EMT gene expression. Thus, it can serve as a potential ERK pathway inhibitor in lung cancer therapeutics.

摘要

背景与目的

ERK 通路是肺癌转移中最重要的通路之一。靶向其通路对肺癌研究具有决定性意义。因此,本研究首次证明了羽扇醇通过干扰 ERK 信号通路对肺癌 A549 细胞具有显著且选择性的抗转移作用。

材料与方法

通过计算机预测羽扇醇的人类蛋白靶标。在体外进行迁移和细胞毒性测定。使用酶联免疫吸附测定法(ELISA)确保 Erk1/2 和 pErk1/2 蛋白的表达水平。使用半定量 RT-PCR 技术估计 N-钙粘蛋白和波形蛋白等关键间质标志物基因表达水平的变化。

结果

羽扇醇被发现可有效靶向 ERK 和 MEK 蛋白。尽管羽扇醇没有细胞毒性作用,但它也显著抑制了 A549 细胞的迁移,同时降低了 pErk1/2 蛋白以及 N-钙粘蛋白和波形蛋白基因的表达。

结论

羽扇醇抑制细胞迁移,对 A549 细胞无细胞毒性作用,降低了 pErk1/2 和 EMT 基因的表达。因此,它可以作为肺癌治疗中潜在的 ERK 通路抑制剂。

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