Evidence map›Paper›PMID 39052060›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2025

Revealing the active ingredients and mechanisms of Xiatianwu against hepatocellular carcinoma: a study based on network pharmacology and bioinformatics.

Hui Wang, Weina Zhang, Liling Li, Hong Wang, Honglin Jiang, Wenna Li, Jinchang Huang, Yuxiang Wan

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hui WangBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China.ORCID 0000-0003-3653-1789
Weina ZhangBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China.
Liling LiBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China.
Hong WangDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100700, China.
Honglin JiangBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China.
Wenna LiBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China.
Jinchang HuangBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China. zryhhuang@163.com.
Yuxiang WanBeijing University of Chinese Medicine Third Affiliated Hospital, Beijing, 100029, China. wanyuxiang@bucm.edu.cn.

Funding

Project of Beijing University of Chinese Medicine 2022-JYB-JBZR-042Project of the China Association of Chinese Medicine CACM-2022-QNRC2-B02the Natural Science Foundation of China 82074545the Natural Science Foundation of China 82205292
6 · The paper itself

Abstract

Xiatianwu is a traditional Chinese medicine. This study investigates the function of Xiatianwu in treating HCC through database analyses and in vitro experiments. The active ingredients of Xiatianwu were identified from TCMSP and HERB databases and their targets were predicted by Swiss TargetPrediction. The HCC dataset was screened using the GEO database, and the differentially expressed genes between HCC and non-tumor liver tissues were analyzed to identify overlapping targets with Xiatianwu. The intersecting targets underwent enrichment analysis using R software to elucidate the molecular mechanisms of Xiatianwu against HCC. Core targets were identified using the PPI network and MCODE algorithm. Clinical relevance and disease prognosis in HCC were verified using the TCGA database. Meanwhile, binding affinities among components and targets were validated with molecular docking. Finally, the anti-HCC efficacy of the active ingredient was validated in vitro. Our findings revealed that eight active ingredients of Xiatianwu interacted with 11 key targets, providing anti-HCC efficacy. Molecular docking indicated that bicuculline and fumarine exhibited superior binding abilities. Bicuculline, a representative ingredient of Xiatianwu, was chosen for in vitro validation. Results demonstrated that bicuculline, in a dose-dependent manner inhibited HCC cell viability, reduced migration, suppressed the G0/M cell cycle, and decreased core protein expression. Xiatianwu demonstrates significant potential for clinical application in treating HCC. Bicuculline, a key active ingredient of Xiatianwu, exerts anti-HCC effects by inhibiting the cell cycle.

Indexed as

Antineoplastic Agents, PhytogenicBicucullineCorydalisDrugs, Chinese HerbalNetwork PharmacologyCarcinoma, HepatocellularCell CycleCell MovementComputational BiologyGene Expression ProfilingHep G2 CellsHumansLiver NeoplasmsMolecular Docking SimulationAntineoplastic Agents, PhytogenicBicucullineDrugs, Chinese HerbalBicucullineBioinformaticsHepatocellular carcinomaNetwork pharmacologyXiatianwu (Rhizoma Corydalis Decumbentis)

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.