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通过谱效关系和蛋白质组学揭示浙贝母治疗非小细胞肺癌的活性成分及作用机制。

Revealing active components and action mechanism of Fritillariae Bulbus against non-small cell lung cancer through spectrum-effect relationship and proteomics.

机构信息

State Key Laboratory of Natural Medicines, China Pharmaceutical University, No. 24 Tongjia Lane, Nanjing 210009, China.

College of Chemical Engineering, Nanjing Forestry University, No. 159 Longpan Road, Nanjing 210037, China.

出版信息

Phytomedicine. 2023 Feb;110:154635. doi: 10.1016/j.phymed.2022.154635. Epub 2022 Dec 26.

Abstract

BACKGROUND

Fritillariae Bulbus (FB) is widely used as a traditional medicine for the treatment of lung meridian diseases. It has been proved that FB has good anti-non-small cell lung cancer (NSCLC) activity. However, the active components and potential mechanism are still not clear.

PURPOSE

To reveal the bioactive components of FB against NSCLC and potential mechanism through spectrum-effect relationship and proteomics.

METHOD

First, the FB extract was chemically profiled by UHPLC-QTOF-MS and the inhibitory effect of FB extract on A549 cell viability was evaluated by Cell Counting Kit-8 assay. Second, orthogonal-partial least squares-regression analysis was applied to screen potential active compounds through correlating the chemical profile with corresponding inhibitory effect. Third, the anti-NSCLC activities of potential active components were further investigated in terms of cell proliferation, cell cycle and cell apoptosis in vitro and tumor growth in vivo. Finally, proteomics was utilized to reveal the underlying anti-NSCLC mechanism.

RESULTS

Six potential active components including verticine, verticinone, zhebeirine, ebeiedinone, yibeissine and peimisine were screened out by spectrum-effect relationship. Among them, zhebeirine showed higher inhibitory effect on A549 cell viability with IC value of 36.93 μM and dosage-dependent inhibition of A549 xenograft tumor growth in nude mice. Proteomics and western blotting assays indicated that zhebeirine could arrest cell cycle by down-regulating the expressions of CDK1, CDK2, Cyclin A2, Cyclin B2 and inhibiting the phosphorylation of p53. Moreover, the proteins participating in p53 signaling pathway including PCNA, 14-3-3σ, CHEK1 were significantly decreased, which suggested that zhebeirine affected cell cycle progression through p53 signaling pathway.

CONCLUSION

This study not only provides scientific evidence to support the clinical application of FB against NSCLC, but also demonstrates that zhebeirine is a promising anti-NSCLC lead compound deserving further studies.

摘要

背景

贝母被广泛用作治疗肺经疾病的传统药物。已经证明贝母对非小细胞肺癌(NSCLC)具有良好的活性。然而,其活性成分和潜在机制仍不清楚。

目的

通过光谱-效关系和蛋白质组学揭示贝母治疗 NSCLC 的生物活性成分和潜在机制。

方法

首先,采用 UHPLC-QTOF-MS 对贝母提取物进行化学分析,并通过细胞计数试剂盒-8 测定法评估贝母提取物对 A549 细胞活力的抑制作用。其次,通过将化学特征与相应的抑制作用相关联,应用正交偏最小二乘回归分析筛选潜在的活性化合物。然后,通过体外细胞增殖、细胞周期和细胞凋亡以及体内肿瘤生长进一步研究潜在活性成分的抗 NSCLC 活性。最后,利用蛋白质组学揭示其潜在的抗 NSCLC 机制。

结果

通过光谱-效关系筛选出 6 种潜在的活性成分,包括浙贝甲素、浙贝乙素、浙贝丙素、伊贝辛酮、异贝母辛和去氢浙贝甲素。其中,浙贝丙素对 A549 细胞活力的抑制作用更强,IC 值为 36.93 μM,对裸鼠 A549 异种移植肿瘤生长具有剂量依赖性抑制作用。蛋白质组学和 Western blotting 分析表明,浙贝丙素通过下调 CDK1、CDK2、Cyclin A2、Cyclin B2 的表达并抑制 p53 的磷酸化来使细胞周期停滞。此外,参与 p53 信号通路的蛋白,包括 PCNA、14-3-3σ、CHEK1 明显减少,表明浙贝丙素通过 p53 信号通路影响细胞周期进程。

结论

本研究不仅为贝母治疗 NSCLC 的临床应用提供了科学依据,还表明浙贝丙素是一种有前途的抗 NSCLC 先导化合物,值得进一步研究。

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