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基于网络药理学和实验验证的 Georgi 调控骨癌痛的机制。

Regulatory mechanism of Georgi on bone cancer pain based on network pharmacology and experimental verification.

机构信息

Inner Mongolia People's Hospital, Hohhot, China.

Inner Mongolia Medical University, Hohhot, China.

出版信息

PeerJ. 2022 Nov 17;10:e14394. doi: 10.7717/peerj.14394. eCollection 2022.

Abstract

CONTEXT

Georgi (SBG) may relieve bone cancer pain (BCP) by regulating cell proliferation, angiogenesis, and apoptosis.

OBJECTIVE

The mechanism of SBG in the treatment of BCP remains to be further explored.

METHODS

The active compounds and targets of SBG were obtained from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) and SwissTargetPrediction databases. BCP-related targets were screened from NCBI and GeneCards databases. Additionally, Cytoscape software was applied to construct network diagrams, and OmicShare platform was used to enrich Gene Ontology (GO) and pathways. Finally, the verification of active compounds and core targets was performed based on quantitative real-time PCR (qRT-PCR).

RESULTS

Interestingly, we identified baicalein and wogonin as the main active components of SBG. A total of 41 SBG targets, including VEGFA, IL6, MAPK3, JUN and TNF, were obtained in the treatment of BCP. In addition, pathways in cancer may be an essential way of SBG in the treatment of BCP. Experimental verification had shown that baicalein and wogonin were significantly related to BCP core targets.

CONCLUSIONS

The active components of SBG have been clarified, and the mechanism of the active components in treating BCP has been predicted and verified, which provides an experimental and theoretical basis for the in-depth elucidation of the pharmacodynamics material basis and mechanism of SBG.

摘要

背景

黄芩(SBG)可能通过调节细胞增殖、血管生成和细胞凋亡来缓解骨癌疼痛(BCP)。

目的

SBG 治疗 BCP 的机制仍需进一步探讨。

方法

从中药系统药理学数据库和分析平台(TCMSP)和 SwissTargetPrediction 数据库中获取 SBG 的活性化合物和靶标。从 NCBI 和 GeneCards 数据库筛选 BCP 相关靶标。此外,使用 Cytoscape 软件构建网络图,并使用 OmicShare 平台进行基因本体(GO)和通路富集。最后,基于实时荧光定量 PCR(qRT-PCR)对活性化合物和核心靶标进行验证。

结果

有趣的是,我们确定黄芩苷和白杨素是 SBG 的主要活性成分。在治疗 BCP 中,共获得 41 个 SBG 靶标,包括 VEGFA、IL6、MAPK3、JUN 和 TNF。此外,癌症通路可能是 SBG 治疗 BCP 的重要途径。实验验证表明,黄芩苷和白杨素与 BCP 核心靶标显著相关。

结论

阐明了 SBG 的活性成分,并预测和验证了活性成分治疗 BCP 的机制,为深入阐明 SBG 的药效物质基础和作用机制提供了实验和理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/342f/9676018/d6e320bab498/peerj-10-14394-g001.jpg

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